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A clinical trial helps researchers to understand if a new drug, a new combination of drugs, surgical procedure, medical device, diagnostic method, prevention method or other treatment is effective for a specific health condition, and is safe to use.

A clinical trial helps researchers to understand if a new drug, a new combination of drugs, surgical procedure, medical device, diagnostic method, prevention method or other treatment is effective for a specific health condition, and is safe to use.

A clinical trial helps researchers to understand if a new drug, a new combination of drugs, surgical procedure, medical device, diagnostic method, prevention method or other treatment is effective for a specific health condition, and is safe to use.

A clinical trial helps researchers to understand if a new drug, a new combination of drugs, surgical procedure, medical device, diagnostic method, prevention method or other treatment is effective for a specific health condition, and is safe to use.

A clinical trial helps researchers to understand if a new drug, a new combination of drugs, surgical procedure, medical device, diagnostic method, prevention method or other treatment is effective for a specific health condition, and is safe to use.

A clinical trial helps researchers to understand if a new drug, a new combination of drugs, surgical procedure, medical device, diagnostic method, prevention method or other treatment is effective for a specific health condition, and is safe to use.

A clinical trial helps researchers to understand if a new drug, a new combination of drugs, surgical procedure, medical device, diagnostic method, prevention method or other treatment is effective for a specific health condition, and is safe to use.

A clinical trial helps researchers to understand if a new drug, a new combination of drugs, surgical procedure, medical device, diagnostic method, prevention method or other treatment is effective for a specific health condition, and is safe to use.

A clinical trial helps researchers to understand if a new drug, a new combination of drugs, surgical procedure, medical device, diagnostic method, prevention method or other treatment is effective for a specific health condition, and is safe to use.

A clinical trial helps researchers to understand if a new drug, a new combination of drugs, surgical procedure, medical device, diagnostic method, prevention method or other treatment is effective for a specific health condition, and is safe to use.

A clinical trial helps researchers to understand if a new drug, a new combination of drugs, surgical procedure, medical device, diagnostic method, prevention method or other treatment is effective for a specific health condition, and is safe to use.

A clinical trial helps researchers to understand if a new drug, a new combination of drugs, surgical procedure, medical device, diagnostic method, prevention method or other treatment is effective for a specific health condition, and is safe to use.

Clinical trials are so important because they’re the only way to see if new drugs, new combinations of drugs, new treatment methods, medical innovations, diagnostic methods or medical devices actually work for a specific health condition and are safe to use. Without clinical trials, there are no advancements in medicine.

The FDA (Food and Drug Administration) regulates clinical trials and demands that clinical trials must be conducted before a new drug, medical device diagnostic methods or other treatments can be marketed in the United States.

Clinical trials are so important because they’re the only way to see if new drugs, new combinations of drugs, new treatment methods, medical innovations, diagnostic methods or medical devices actually work for a specific health condition and are safe to use. Without clinical trials, there are no advancements in medicine.

The FDA (Food and Drug Administration) regulates clinical trials and demands that clinical trials must be conducted before a new drug, medical device diagnostic methods or other treatments can be marketed in the United States.

Clinical trials are so important because they’re the only way to see if new drugs, new combinations of drugs, new treatment methods, medical innovations, diagnostic methods or medical devices actually work for a specific health condition and are safe to use. Without clinical trials, there are no advancements in medicine.

The FDA (Food and Drug Administration) regulates clinical trials and demands that clinical trials must be conducted before a new drug, medical device diagnostic methods or other treatments can be marketed in the United States.

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Clinical trials are so important because they’re the only way to see if new drugs, new combinations of drugs, new treatment methods, medical innovations, diagnostic methods or medical devices actually work for a specific health condition and are safe to use. Without clinical trials, there are no advancements in medicine.

The FDA (Food and Drug Administration) regulates clinical trials and demands that clinical trials must be conducted before a new drug, medical device diagnostic methods or other treatments can be marketed in the United States.

Clinical trials are so important because they’re the only way to see if new drugs, new combinations of drugs, new treatment methods, medical innovations, diagnostic methods or medical devices actually work for a specific health condition and are safe to use. Without clinical trials, there are no advancements in medicine.

The FDA (Food and Drug Administration) regulates clinical trials and demands that clinical trials must be conducted before a new drug, medical device diagnostic methods or other treatments can be marketed in the United States.

Clinical trials are so important because they’re the only way to see if new drugs, new combinations of drugs, new treatment methods, medical innovations, diagnostic methods or medical devices actually work for a specific health condition and are safe to use. Without clinical trials, there are no advancements in medicine.

The FDA (Food and Drug Administration) regulates clinical trials and demands that clinical trials must be conducted before a new drug, medical device diagnostic methods or other treatments can be marketed in the United States.

Clinical trials are so important because they’re the only way to see if new drugs, new combinations of drugs, new treatment methods, medical innovations, diagnostic methods or medical devices actually work for a specific health condition and are safe to use. Without clinical trials, there are no advancements in medicine.

The FDA (Food and Drug Administration) regulates clinical trials and demands that clinical trials must be conducted before a new drug, medical device diagnostic methods or other treatments can be marketed in the United States.

Clinical trials are so important because they’re the only way to see if new drugs, new combinations of drugs, new treatment methods, medical innovations, diagnostic methods or medical devices actually work for a specific health condition and are safe to use. Without clinical trials, there are no advancements in medicine.

The FDA (Food and Drug Administration) regulates clinical trials and demands that clinical trials must be conducted before a new drug, medical device diagnostic methods or other treatments can be marketed in the United States.

Clinical trials are so important because they’re the only way to see if new drugs, new combinations of drugs, new treatment methods, medical innovations, diagnostic methods or medical devices actually work for a specific health condition and are safe to use. Without clinical trials, there are no advancements in medicine.

The FDA (Food and Drug Administration) regulates clinical trials and demands that clinical trials must be conducted before a new drug, medical device diagnostic methods or other treatments can be marketed in the United States.

Clinical trials are so important because they’re the only way to see if new drugs, new combinations of drugs, new treatment methods, medical innovations, diagnostic methods or medical devices actually work for a specific health condition and are safe to use. Without clinical trials, there are no advancements in medicine.

The FDA (Food and Drug Administration) regulates clinical trials and demands that clinical trials must be conducted before a new drug, medical device diagnostic methods or other treatments can be marketed in the United States.

Clinical trials are so important because they’re the only way to see if new drugs, new combinations of drugs, new treatment methods, medical innovations, diagnostic methods or medical devices actually work for a specific health condition and are safe to use. Without clinical trials, there are no advancements in medicine.

The FDA (Food and Drug Administration) regulates clinical trials and demands that clinical trials must be conducted before a new drug, medical device diagnostic methods or other treatments can be marketed in the United States.

Clinical trials are so important because they’re the only way to see if new drugs, new combinations of drugs, new treatment methods, medical innovations, diagnostic methods or medical devices actually work for a specific health condition and are safe to use. Without clinical trials, there are no advancements in medicine.

The FDA (Food and Drug Administration) regulates clinical trials and demands that clinical trials must be conducted before a new drug, medical device diagnostic methods or other treatments can be marketed in the United States.

If you wish to volunteer in a clinical trial, you agree to participate and test new drugs, new treatment methods, new diagnostic methods or new medical devices, for example. Important: nobody can force you to participate in a clinical trial and you can drop out at any time, even when you’re already enrolled in a clinical trial.

You should consider the following questions when thinking about joining a clinical trial:

Will the research help me?

What are the risks involved?

What do I need to do? E.g. how many doctor visits are involved? Do I have to change something in my lifestyle?

Will I be compensated?

If you wish to volunteer in a clinical trial, you agree to participate and test new drugs, new treatment methods, new diagnostic methods or new medical devices, for example. Important: nobody can force you to participate in a clinical trial and you can drop out at any time, even when you’re already enrolled in a clinical trial.

You should consider the following questions when thinking about joining a clinical trial:

Will the research help me?

What are the risks involved?

What do I need to do? E.g. how many doctor visits are involved? Do I have to change something in my lifestyle?

Will I be compensated?

If you wish to volunteer in a clinical trial, you agree to participate and test new drugs, new treatment methods, new diagnostic methods or new medical devices, for example. Important: nobody can force you to participate in a clinical trial and you can drop out at any time, even when you’re already enrolled in a clinical trial.

You should consider the following questions when thinking about joining a clinical trial:

Will the research help me?

What are the risks involved?

What do I need to do? E.g. how many doctor visits are involved? Do I have to change something in my lifestyle?

Will I be compensated?

If you wish to volunteer in a clinical trial, you agree to participate and test new drugs, new treatment methods, new diagnostic methods or new medical devices, for example. Important: nobody can force you to participate in a clinical trial and you can drop out at any time, even when you’re already enrolled in a clinical trial.

You should consider the following questions when thinking about joining a clinical trial:

Will the research help me?

What are the risks involved?

What do I need to do? E.g. how many doctor visits are involved? Do I have to change something in my lifestyle?

Will I be compensated?

If you wish to volunteer in a clinical trial, you agree to participate and test new drugs, new treatment methods, new diagnostic methods or new medical devices, for example. Important: nobody can force you to participate in a clinical trial and you can drop out at any time, even when you’re already enrolled in a clinical trial.

You should consider the following questions when thinking about joining a clinical trial:

Will the research help me?

What are the risks involved?

What do I need to do? E.g. how many doctor visits are involved? Do I have to change something in my lifestyle?

Will I be compensated?

This is a tough question to answer in a general way, because expectations differ from study to study. Some clinical trials expect that you take some supplements and visit the research site closest to you every month. Others expect that you go to the gym 3-4 times per week, others expect that you change your diet.

Generally, you should ask the clinical trial team what the time commitment is for the clinical trial you’re interested in, and what is expected from you.

If you wish to volunteer in a clinical trial, you agree to participate and test new drugs, new treatment methods, new diagnostic methods or new medical devices, for example. Important: nobody can force you to participate in a clinical trial and you can drop out at any time, even when you’re already enrolled in a clinical trial.

You should consider the following questions when thinking about joining a clinical trial:

Will the research help me?

What are the risks involved?

What do I need to do? E.g. how many doctor visits are involved? Do I have to change something in my lifestyle?

Will I be compensated?

If you wish to volunteer in a clinical trial, you agree to participate and test new drugs, new treatment methods, new diagnostic methods or new medical devices, for example. Important: nobody can force you to participate in a clinical trial and you can drop out at any time, even when you’re already enrolled in a clinical trial.

You should consider the following questions when thinking about joining a clinical trial:

Will the research help me?

What are the risks involved?

What do I need to do? E.g. how many doctor visits are involved? Do I have to change something in my lifestyle?

Will I be compensated?

If you wish to volunteer in a clinical trial, you agree to participate and test new drugs, new treatment methods, new diagnostic methods or new medical devices, for example. Important: nobody can force you to participate in a clinical trial and you can drop out at any time, even when you’re already enrolled in a clinical trial.

You should consider the following questions when thinking about joining a clinical trial:

Will the research help me?

What are the risks involved?

What do I need to do? E.g. how many doctor visits are involved? Do I have to change something in my lifestyle?

Will I be compensated?

If you wish to volunteer in a clinical trial, you agree to participate and test new drugs, new treatment methods, new diagnostic methods or new medical devices, for example. Important: nobody can force you to participate in a clinical trial and you can drop out at any time, even when you’re already enrolled in a clinical trial.

You should consider the following questions when thinking about joining a clinical trial:

Will the research help me?

What are the risks involved?

What do I need to do? E.g. how many doctor visits are involved? Do I have to change something in my lifestyle?

Will I be compensated?

If you wish to volunteer in a clinical trial, you agree to participate and test new drugs, new treatment methods, new diagnostic methods or new medical devices, for example. Important: nobody can force you to participate in a clinical trial and you can drop out at any time, even when you’re already enrolled in a clinical trial.

You should consider the following questions when thinking about joining a clinical trial:

Will the research help me?

What are the risks involved?

What do I need to do? E.g. how many doctor visits are involved? Do I have to change something in my lifestyle?

Will I be compensated?

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5. Das war's! Eine Miniaturansicht Ihres Video wird in der Antwort-Textbox erscheinen

If you wish to volunteer in a clinical trial, you agree to participate and test new drugs, new treatment methods, new diagnostic methods or new medical devices, for example. Important: nobody can force you to participate in a clinical trial and you can drop out at any time, even when you’re already enrolled in a clinical trial.

You should consider the following questions when thinking about joining a clinical trial:

- Will the research help me?

- What are the risks involved?

- What do I need to do? E.g. how many doctor visits are involved?

- Do I have to change something in my lifestyle?

- Will I be compensated?

This is a tough question to answer in a general way, because expectations differ from study to study. Some clinical trials expect that you take some supplements and visit the research site closest to you every month. Others expect that you go to the gym 3-4 times per week, others expect that you change your diet.

Generally, you should ask the clinical trial team what the time commitment is for the clinical trial you’re interested in, and what is expected from you.

This is a tough question to answer in a general way, because expectations differ from study to study. Some clinical trials expect that you take some supplements and visit the research site closest to you every month. Others expect that you go to the gym 3-4 times per week, others expect that you change your diet.

Generally, you should ask the clinical trial team what the time commitment is for the clinical trial you’re interested in, and what is expected from you.

Der FAQ-Titel kann in den App-Einstellungen angepasst werden. Löschen Sie den Titel, indem Sie die Markierung im Kontrollkästchen entfernen.

This is a tough question to answer in a general way, because expectations differ from study to study. Some clinical trials expect that you take some supplements and visit the research site closest to you every month. Others expect that you go to the gym 3-4 times per week, others expect that you change your diet.

Generally, you should ask the clinical trial team what the time commitment is for the clinical trial you’re interested in, and what is expected from you.

If you wish to volunteer in a clinical trial, you agree to participate and test new drugs, new treatment methods, new diagnostic methods or new medical devices, for example. Important: nobody can force you to participate in a clinical trial and you can drop out at any time, even when you’re already enrolled in a clinical trial.

You should consider the following questions when thinking about joining a clinical trial:

Will the research help me?

What are the risks involved?

What do I need to do? E.g. how many doctor visits are involved? Do I have to change something in my lifestyle?

Will I be compensated?

This is a tough question to answer in a general way, because expectations differ from study to study. Some clinical trials expect that you take some supplements and visit the research site closest to you every month. Others expect that you go to the gym 3-4 times per week, others expect that you change your diet.

Generally, you should ask the clinical trial team what the time commitment is for the clinical trial you’re interested in, and what is expected from you.

This is a tough question to answer in a general way, because expectations differ from study to study. Some clinical trials expect that you take some supplements and visit the research site closest to you every month. Others expect that you go to the gym 3-4 times per week, others expect that you change your diet.

Generally, you should ask the clinical trial team what the time commitment is for the clinical trial you’re interested in, and what is expected from you.

This is a tough question to answer in a general way, because expectations differ from study to study. Some clinical trials expect that you take some supplements and visit the research site closest to you every month. Others expect that you go to the gym 3-4 times per week, others expect that you change your diet.

Generally, you should ask the clinical trial team what the time commitment is for the clinical trial you’re interested in, and what is expected from you.

This is a tough question to answer in a general way, because expectations differ from study to study. Some clinical trials expect that you take some supplements and visit the research site closest to you every month. Others expect that you go to the gym 3-4 times per week, others expect that you change your diet.

Generally, you should ask the clinical trial team what the time commitment is for the clinical trial you’re interested in, and what is expected from you.

This is a tough question to answer in a general way, because expectations differ from study to study. Some clinical trials expect that you take some supplements and visit the research site closest to you every month. Others expect that you go to the gym 3-4 times per week, others expect that you change your diet.

Generally, you should ask the clinical trial team what the time commitment is for the clinical trial you’re interested in, and what is expected from you.

This is a tough question to answer in a general way, because expectations differ from study to study. Some clinical trials expect that you take some supplements and visit the research site closest to you every month. Others expect that you go to the gym 3-4 times per week, others expect that you change your diet.

Generally, you should ask the clinical trial team what the time commitment is for the clinical trial you’re interested in, and what is expected from you.

This is a tough question to answer in a general way, because expectations differ from study to study. Some clinical trials expect that you take some supplements and visit the research site closest to you every month. Others expect that you go to the gym 3-4 times per week, others expect that you change your diet.

Generally, you should ask the clinical trial team what the time commitment is for the clinical trial you’re interested in, and what is expected from you.

This is a tough question to answer in a general way, because expectations differ from study to study. Some clinical trials expect that you take some supplements and visit the research site closest to you every month. Others expect that you go to the gym 3-4 times per week, others expect that you change your diet.

Generally, you should ask the clinical trial team what the time commitment is for the clinical trial you’re interested in, and what is expected from you.

You can find clinical trials directly via www.clinicaltrials.gov, but you can also sign up with Citruslabs and we automatically match you with a clinical trial in your area that fits your needs.

You can find clinical trials directly via www.clinicaltrials.gov, but you can also sign up with Citruslabs and we automatically match you with a clinical trial in your area that fits your needs.

You can find clinical trials directly via www.clinicaltrials.gov, but you can also sign up with Citruslabs and we automatically match you with a clinical trial in your area that fits your needs.

You can find clinical trials directly via www.clinicaltrials.gov, but you can also sign up with Citruslabs and we automatically match you with a clinical trial in your area that fits your needs.

You can find clinical trials directly via www.clinicaltrials.gov, but you can also sign up with Citruslabs and we automatically match you with a clinical trial in your area that fits your needs.

You can find clinical trials directly via www.clinicaltrials.gov, but you can also sign up with Citruslabs and we automatically match you with a clinical trial in your area that fits your needs.

You can find clinical trials directly via www.clinicaltrials.gov, but you can also sign up with Citruslabs and we automatically match you with a clinical trial in your area that fits your needs.

You can find clinical trials directly via www.clinicaltrials.gov, but you can also sign up with Citruslabs and we automatically match you with a clinical trial in your area that fits your needs.

You can find clinical trials directly via www.clinicaltrials.gov, but you can also sign up with Citruslabs and we automatically match you with a clinical trial in your area that fits your needs.

You can find clinical trials directly via www.clinicaltrials.gov, but you can also sign up with Citruslabs and we automatically match you with a clinical trial in your area that fits your needs.

You can find clinical trials directly via www.clinicaltrials.gov, but you can also sign up with Citruslabs and we automatically match you with a clinical trial in your area that fits your needs.

When you expressed interest in joining a clinical trial via Citruslabs, our algorithm checks if you qualify for any of the clinical trials we are working with and matches you with the closest research site (usually up to 25 miles away from you - in highly populated areas usually up to 10 miles).

The research team from the research site will then give you a call to tell you more about the clinical trial and also ask you some additional questions. If everything works for you, they will invite you to an on-site screening visit at their location. Often these visits include blood pressure measurement, heart rate measurement, urine analysis, and maybe some blood work. All this is free of charge for you.

Once you passed the screening, the site will invite you to join the clinical trial and needs you to sign an informed consent form to do this. The informed consent form gives you all the information about the purpose of the clinical trial, benefits and potential risks, and helps you to better understand what to expect when you participate in this specific trial.

Alzheimer’s is the most common type of dementia, and as yet its exact cause is unknown. During the course of the disease, proteins build up in the brain, making ‘tangles’ which sever the connection between nerve cells, eventually leading to the death of nerve cells and a loss of brain tissue. Developing Alzheimer’s has no direct link with vascular problems such as suffering a stroke or a heart attack. What is known, is that your risk of developing Alzheimer’s increases with age. In the early stages of the disease, people might have vision, word finding, and spatial difficulties. It can also cause changes in judgement and reasoning, with people often exercising poor judgement during day to day tasks. Currently, there is no cure for Alzheimer’s Disease, but drugs such as Donepezil are often prescribed to help alleviate memory problems and improve concentration, making daily tasks and living much easier.

When you expressed interest in joining a clinical trial via Citruslabs, our algorithm checks if you qualify for any of the clinical trials we are working with and matches you with the closest research site (usually up to 25 miles away from you - in highly populated areas usually up to 10 miles).

The research team from the research site will then give you a call to tell you more about the clinical trial and also ask you some additional questions. If everything works for you, they will invite you to an on-site screening visit at their location. Often these visits include blood pressure measurement, heart rate measurement, urine analysis, and maybe some blood work. All this is free of charge for you.

Once you passed the screening, the site will invite you to join the clinical trial and needs you to sign an informed consent form to do this. The informed consent form gives you all the information about the purpose of the clinical trial, benefits and potential risks, and helps you to better understand what to expect when you participate in this specific trial.

When you expressed interest in joining a clinical trial via Citruslabs, our algorithm checks if you qualify for any of the clinical trials we are working with and matches you with the closest research site (usually up to 25 miles away from you - in highly populated areas usually up to 10 miles).

The research team from the research site will then give you a call to tell you more about the clinical trial and also ask you some additional questions. If everything works for you, they will invite you to an on-site screening visit at their location. Often these visits include blood pressure measurement, heart rate measurement, urine analysis, and maybe some blood work. All this is free of charge for you.

Once you passed the screening, the site will invite you to join the clinical trial and needs you to sign an informed consent form to do this. The informed consent form gives you all the information about the purpose of the clinical trial, benefits and potential risks, and helps you to better understand what to expect when you participate in this specific trial.

Benefits and risks differ from trial to trial and you should always talk to the research team before you decide to participate in a clinical trial to fully understand specific benefits and risks.

Generally, clinical trials may give you access to the best possible treatment for your specific health condition that would otherwise not be available to you. You will also receive attention from a care team consisting of nurses, doctors, and other medical staff, that you would otherwise not get. And, you will help not only research to improve or even find new treatments but as a result, you will also help millions of other people who may be benefitting from these (often live-saving) new treatments in the future as well.

General risks always include possible side effects - that sometimes even need medical attention. If you are part of a randomized trial, this could also mean that there is a placebo (inactive treatment) involved and you could actually get the placebo instead of the real treatment. Or, the trial simply expects too much time commitment from your side.

When you expressed interest in joining a clinical trial via Citruslabs, our algorithm checks if you qualify for any of the clinical trials we are working with and matches you with the closest research site (usually up to 25 miles away from you - in highly populated areas usually up to 10 miles).

The research team from the research site will then give you a call to tell you more about the clinical trial and also ask you some additional questions. If everything works for you, they will invite you to an on-site screening visit at their location. Often these visits include blood pressure measurement, heart rate measurement, urine analysis, and maybe some blood work. All this is free of charge for you.

Once you passed the screening, the site will invite you to join the clinical trial and needs you to sign an informed consent form to do this. The informed consent form gives you all the information about the purpose of the clinical trial, benefits and potential risks, and helps you to better understand what to expect when you participate in this specific trial.

When you expressed interest in joining a clinical trial via Citruslabs, our algorithm checks if you qualify for any of the clinical trials we are working with and matches you with the closest research site (usually up to 25 miles away from you - in highly populated areas usually up to 10 miles).

The research team from the research site will then give you a call to tell you more about the clinical trial and also ask you some additional questions. If everything works for you, they will invite you to an on-site screening visit at their location. Often these visits include blood pressure measurement, heart rate measurement, urine analysis, and maybe some blood work. All this is free of charge for you.

Once you passed the screening, the site will invite you to join the clinical trial and needs you to sign an informed consent form to do this. The informed consent form gives you all the information about the purpose of the clinical trial, benefits and potential risks, and helps you to better understand what to expect when you participate in this specific trial.

When you expressed interest in joining a clinical trial via Citruslabs, our algorithm checks if you qualify for any of the clinical trials we are working with and matches you with the closest research site (usually up to 25 miles away from you - in highly populated areas usually up to 10 miles).

The research team from the research site will then give you a call to tell you more about the clinical trial and also ask you some additional questions. If everything works for you, they will invite you to an on-site screening visit at their location. Often these visits include blood pressure measurement, heart rate measurement, urine analysis, and maybe some blood work. All this is free of charge for you.

Once you passed the screening, the site will invite you to join the clinical trial and needs you to sign an informed consent form to do this. The informed consent form gives you all the information about the purpose of the clinical trial, benefits and potential risks, and helps you to better understand what to expect when you participate in this specific trial.

When you expressed interest in joining a clinical trial via Citruslabs, our algorithm checks if you qualify for any of the clinical trials we are working with and matches you with the closest research site (usually up to 25 miles away from you - in highly populated areas usually up to 10 miles).

The research team from the research site will then give you a call to tell you more about the clinical trial and also ask you some additional questions. If everything works for you, they will invite you to an on-site screening visit at their location. Often these visits include blood pressure measurement, heart rate measurement, urine analysis, and maybe some blood work. All this is free of charge for you.

Once you passed the screening, the site will invite you to join the clinical trial and needs you to sign an informed consent form to do this. The informed consent form gives you all the information about the purpose of the clinical trial, benefits and potential risks, and helps you to better understand what to expect when you participate in this specific trial.

When you expressed interest in joining a clinical trial via Citruslabs, our algorithm checks if you qualify for any of the clinical trials we are working with and matches you with the closest research site (usually up to 25 miles away from you - in highly populated areas usually up to 10 miles).

The research team from the research site will then give you a call to tell you more about the clinical trial and also ask you some additional questions. If everything works for you, they will invite you to an on-site screening visit at their location. Often these visits include blood pressure measurement, heart rate measurement, urine analysis, and maybe some blood work. All this is free of charge for you.

Once you passed the screening, the site will invite you to join the clinical trial and needs you to sign an informed consent form to do this. The informed consent form gives you all the information about the purpose of the clinical trial, benefits and potential risks, and helps you to better understand what to expect when you participate in this specific trial.

Vascular dementia is the second most common form of dementia after Alzheimer’s disease. It is caused by a lack of blood flow to the brain, often due to a blockage in the veins leading to the brain. Separate conditions that prevent blood flowing to the brain can often lead to vascular dementia, such as a stroke, aneurysm or heart attack. Depriving the brain of oxygen in this way leads to brain damage, which can occur suddenly or over a longer period of time. The way vascular dementia manifests itself can vary depending on which part of the brain is affected, and its severity depends on how long the brain was deprived of oxygen and blood. Common symptoms include difficulty with reasoning and judgement, confusion and memory problems, unsteady gait and difficulty controlling urination/needing to urinate more frequently. There is no way to fully reverse vascular dementia. However, taking medication to control blood pressure and cholesterol and adopting a healthier lifestyle can help repair parts of the brain, preventing future heart attacks or strokes which would worsen the condition.

When you expressed interest in joining a clinical trial via Citruslabs, our algorithm checks if you qualify for any of the clinical trials we are working with and matches you with the closest research site (usually up to 25 miles away from you - in highly populated areas usually up to 10 miles).

The research team from the research site will then give you a call to tell you more about the clinical trial and also ask you some additional questions. If everything works for you, they will invite you to an on-site screening visit at their location. Often these visits include blood pressure measurement, heart rate measurement, urine analysis, and maybe some blood work. All this is free of charge for you.

Once you passed the screening, the site will invite you to join the clinical trial and needs you to sign an informed consent form to do this. The informed consent form gives you all the information about the purpose of the clinical trial, benefits and potential risks, and helps you to better understand what to expect when you participate in this specific trial.

When you expressed interest in joining a clinical trial via Citruslabs, our algorithm checks if you qualify for any of the clinical trials we are working with and matches you with the closest research site (usually up to 25 miles away from you - in highly populated areas usually up to 10 miles).

The research team from the research site will then give you a call to tell you more about the clinical trial and also ask you some additional questions. If everything works for you, they will invite you to an on-site screening visit at their location. Often these visits include blood pressure measurement, heart rate measurement, urine analysis, and maybe some blood work. All this is free of charge for you.

Once you passed the screening, the site will invite you to join the clinical trial and needs you to sign an informed consent form to do this. The informed consent form gives you all the information about the purpose of the clinical trial, benefits and potential risks, and helps you to better understand what to expect when you participate in this specific trial.

When you expressed interest in joining a clinical trial via Citruslabs, our algorithm checks if you qualify for any of the clinical trials we are working with and matches you with the closest research site (usually up to 25 miles away from you - in highly populated areas usually up to 10 miles).

The research team from the research site will then give you a call to tell you more about the clinical trial and also ask you some additional questions. If everything works for you, they will invite you to an on-site screening visit at their location. Often these visits include blood pressure measurement, heart rate measurement, urine analysis, and maybe some blood work. All this is free of charge for you.

Once you passed the screening, the site will invite you to join the clinical trial and needs you to sign an informed consent form to do this. The informed consent form gives you all the information about the purpose of the clinical trial, benefits and potential risks, and helps you to better understand what to expect when you participate in this specific trial.

Benefits and risks differ from trial to trial and you should always talk to the research team before you decide to participate in a clinical trial to fully understand specific benefits and risks.

Generally, clinical trials may give you access to the best possible treatment for your specific health condition that would otherwise not be available to you. You will also receive attention from a care team consisting of nurses, doctors, and other medical staff, that you would otherwise not get. And, you will help not only research to improve or even find new treatments but as a result, you will also help millions of other people who may be benefitting from these (often live-saving) new treatments in the future as well.

General risks always include possible side effects - that sometimes even need medical attention. If you are part of a randomized trial, this could also mean that there is a placebo (inactive treatment) involved and you could actually get the placebo instead of the real treatment. Or, the trial simply expects too much time commitment from your side.

Benefits and risks differ from trial to trial and you should always talk to the research team before you decide to participate in a clinical trial to fully understand specific benefits and risks.

Generally, clinical trials may give you access to the best possible treatment for your specific health condition that would otherwise not be available to you. You will also receive attention from a care team consisting of nurses, doctors, and other medical staff, that you would otherwise not get. And, you will help not only research to improve or even find new treatments but as a result, you will also help millions of other people who may be benefitting from these (often live-saving) new treatments in the future as well.

General risks always include possible side effects - that sometimes even need medical attention. If you are part of a randomized trial, this could also mean that there is a placebo (inactive treatment) involved and you could actually get the placebo instead of the real treatment. Or, the trial simply expects too much time commitment from your side.

When you expressed interest in joining a clinical trial via Citruslabs, our algorithm checks if you qualify for any of the clinical trials we are working with and matches you with the closest research site (usually up to 25 miles away from you - in highly populated areas usually up to 10 miles).

The research team from the research site will then give you a call to tell you more about the clinical trial and also ask you some additional questions. If everything works for you, they will invite you to an on-site screening visit at their location. Often these visits include blood pressure measurement, heart rate measurement, urine analysis, and maybe some blood work. All this is free of charge for you.

Once you passed the screening, the site will invite you to join the clinical trial and needs you to sign an informed consent form to do this. The informed consent form gives you all the information about the purpose of the clinical trial, benefits and potential risks, and helps you to better understand what to expect when you participate in this specific trial.

Benefits and risks differ from trial to trial and you should always talk to the research team before you decide to participate in a clinical trial to fully understand specific benefits and risks.

Generally, clinical trials may give you access to the best possible treatment for your specific health condition that would otherwise not be available to you. You will also receive attention from a care team consisting of nurses, doctors, and other medical staff, that you would otherwise not get. And, you will help not only research to improve or even find new treatments but as a result, you will also help millions of other people who may be benefitting from these (often live-saving) new treatments in the future as well.

General risks always include possible side effects - that sometimes even need medical attention. If you are part of a randomized trial, this could also mean that there is a placebo (inactive treatment) involved and you could actually get the placebo instead of the real treatment. Or, the trial simply expects too much time commitment from your side.

Benefits and risks differ from trial to trial and you should always talk to the research team before you decide to participate in a clinical trial to fully understand specific benefits and risks.

Generally, clinical trials may give you access to the best possible treatment for your specific health condition that would otherwise not be available to you. You will also receive attention from a care team consisting of nurses, doctors, and other medical staff, that you would otherwise not get. And, you will help not only research to improve or even find new treatments but as a result, you will also help millions of other people who may be benefitting from these (often live-saving) new treatments in the future as well.

General risks always include possible side effects - that sometimes even need medical attention. If you are part of a randomized trial, this could also mean that there is a placebo (inactive treatment) involved and you could actually get the placebo instead of the real treatment. Or, the trial simply expects too much time commitment from your side.

When you express interest in participating in a clinical trial, you have to undergo a screening process in order to determine if you actually qualify to participate in the trial. There is a protocol that sets the rules around who can and who cannot participate.

First, you will undergo a pre-screening that usually happens via phone. Here, the trial staff will ask you specific questions about your demographic information and medical history. They will also provide you with more information on the trial. If the clinical trial staff determined that you meet the criteria that are set by the protocol, you will be invited for an on-site screening visit.

At the on-site screening visit, you will go to the clinical trial location (usually in your area). The clinical trial staff will again give you more information on the trial and a qualified doctor will usually perform a physical examination as well and review your medical history.

Benefits and risks differ from trial to trial and you should always talk to the research team before you decide to participate in a clinical trial to fully understand specific benefits and risks.

Generally, clinical trials may give you access to the best possible treatment for your specific health condition that would otherwise not be available to you. You will also receive attention from a care team consisting of nurses, doctors, and other medical staff, that you would otherwise not get. And, you will help not only research to improve or even find new treatments but as a result, you will also help millions of other people who may be benefitting from these (often live-saving) new treatments in the future as well.

General risks always include possible side effects - that sometimes even need medical attention. If you are part of a randomized trial, this could also mean that there is a placebo (inactive treatment) involved and you could actually get the placebo instead of the real treatment. Or, the trial simply expects too much time commitment from your side.

Benefits and risks differ from trial to trial and you should always talk to the research team before you decide to participate in a clinical trial to fully understand specific benefits and risks.

Generally, clinical trials may give you access to the best possible treatment for your specific health condition that would otherwise not be available to you. You will also receive attention from a care team consisting of nurses, doctors, and other medical staff, that you would otherwise not get. And, you will help not only research to improve or even find new treatments but as a result, you will also help millions of other people who may be benefitting from these (often live-saving) new treatments in the future as well.

General risks always include possible side effects - that sometimes even need medical attention. If you are part of a randomized trial, this could also mean that there is a placebo (inactive treatment) involved and you could actually get the placebo instead of the real treatment. Or, the trial simply expects too much time commitment from your side.

Benefits and risks differ from trial to trial and you should always talk to the research team before you decide to participate in a clinical trial to fully understand specific benefits and risks.

Generally, clinical trials may give you access to the best possible treatment for your specific health condition that would otherwise not be available to you. You will also receive attention from a care team consisting of nurses, doctors, and other medical staff, that you would otherwise not get. And, you will help not only research to improve or even find new treatments but as a result, you will also help millions of other people who may be benefitting from these (often live-saving) new treatments in the future as well.

General risks always include possible side effects - that sometimes even need medical attention. If you are part of a randomized trial, this could also mean that there is a placebo (inactive treatment) involved and you could actually get the placebo instead of the real treatment. Or, the trial simply expects too much time commitment from your side.

Benefits and risks differ from trial to trial and you should always talk to the research team before you decide to participate in a clinical trial to fully understand specific benefits and risks.

Generally, clinical trials may give you access to the best possible treatment for your specific health condition that would otherwise not be available to you. You will also receive attention from a care team consisting of nurses, doctors, and other medical staff, that you would otherwise not get. And, you will help not only research to improve or even find new treatments but as a result, you will also help millions of other people who may be benefitting from these (often live-saving) new treatments in the future as well.

General risks always include possible side effects - that sometimes even need medical attention. If you are part of a randomized trial, this could also mean that there is a placebo (inactive treatment) involved and you could actually get the placebo instead of the real treatment. Or, the trial simply expects too much time commitment from your side.

Dementia with Lewy Bodies (DLB) accounts for about 10-15% of dementia cases. Lewy bodies are tiny deposits of a protein called alpha-synuclein, which appear in nerve cells in the brain. The exact cause of the presence of Lewy bodies in the brain is unknown. Lewy Bodies are the cause of both DLB and Parkinson’s Disease, conditions which affect the brain and nervous system and get worse over time. The way someone is affected by DLB will depend partly on where the Lewy bodies are in the brain. If they are present at the base of the brain, they are closely linked to problems with movement (motor symptoms). These are the main feature of Parkinson's disease. Lewy bodies in the outer layers of the brain are linked to problems with mental abilities (cognitive symptoms), which is a feature of DLB. There is no cure for DLB, and due to the wide range of symptoms which present in patients, it is difficult to prescribe drugs as treatment, so it is advised that people with DLB seek advice from a variety of professionals so that they can manage the disease without drugs.

Benefits and risks differ from trial to trial and you should always talk to the research team before you decide to participate in a clinical trial to fully understand specific benefits and risks.

Generally, clinical trials may give you access to the best possible treatment for your specific health condition that would otherwise not be available to you. You will also receive attention from a care team consisting of nurses, doctors, and other medical staff, that you would otherwise not get. And, you will help not only research to improve or even find new treatments but as a result, you will also help millions of other people who may be benefitting from these (often live-saving) new treatments in the future as well.

General risks always include possible side effects - that sometimes even need medical attention. If you are part of a randomized trial, this could also mean that there is a placebo (inactive treatment) involved and you could actually get the placebo instead of the real treatment. Or, the trial simply expects too much time commitment from your side.

A protocol is a central information source and describes the rules of the clinical trial. First, it states why a specific question is researched and how the research team will answer the question; second, it includes information on the specific procedures, which medications will be used (if any), which data analysis methods will be used, possible benefits and risks and possible adverse events, and third, it also tells you who can and cannot participate. A protocol also tells you how the research team will protect the health and wellbeing of the participants.

A protocol is a central information source and describes the rules of the clinical trial. First, it states why a specific question is researched and how the research team will answer the question; second, it includes information on the specific procedures, which medications will be used (if any), which data analysis methods will be used, possible benefits and risks and possible adverse events, and third, it also tells you who can and cannot participate. A protocol also tells you how the research team will protect the health and wellbeing of the participants.

A protocol is a central information source and describes the rules of the clinical trial. First, it states why a specific question is researched and how the research team will answer the question; second, it includes information on the specific procedures, which medications will be used (if any), which data analysis methods will be used, possible benefits and risks and possible adverse events, and third, it also tells you who can and cannot participate. A protocol also tells you how the research team will protect the health and wellbeing of the participants.

A protocol is a central information source and describes the rules of the clinical trial. First, it states why a specific question is researched and how the research team will answer the question; second, it includes information on the specific procedures, which medications will be used (if any), which data analysis methods will be used, possible benefits and risks and possible adverse events, and third, it also tells you who can and cannot participate. A protocol also tells you how the research team will protect the health and wellbeing of the participants.

Usually, only blinded trials use a placebo, which is an inactive drug or treatment, sometimes also referred to as a “sugar pill”. If you take the placebo, you are in the control group and the goal behind that is to see how the researched drug or treatment compares to the placebo.

Usually, participants in a clinical trial get reimbursed for their travel expenses and time.

A protocol is a central information source and describes the rules of the clinical trial. First, it states why a specific question is researched and how the research team will answer the question; second, it includes information on the specific procedures, which medications will be used (if any), which data analysis methods will be used, possible benefits and risks and possible adverse events, and third, it also tells you who can and cannot participate. A protocol also tells you how the research team will protect the health and wellbeing of the participants.

A protocol is a central information source and describes the rules of the clinical trial. First, it states why a specific question is researched and how the research team will answer the question; second, it includes information on the specific procedures, which medications will be used (if any), which data analysis methods will be used, possible benefits and risks and possible adverse events, and third, it also tells you who can and cannot participate. A protocol also tells you how the research team will protect the health and wellbeing of the participants.

Parkinson's disease dementia is an impairment in thinking and reasoning that eventually affects many people with Parkinson's disease. Parkinson’s is a progressive neurological condition, meaning that it gets worse over time. The three main symptoms of Parkinson’s disease are tremors, slowness of movement and muscle stiffness. As Parkinson's brain changes gradually spread, they often begin to affect mental functions, including memory and the ability to pay attention. People with Parkinson’s disease also have a build up of Lewy bodies in their brains, which are the root cause of the condition, as is the case with Dementia with Lewy bodies. Like DLB, Parkinson’s disease dementia affects each individual differently, so there is no catch-all treatment.

A protocol is a central information source and describes the rules of the clinical trial. First, it states why a specific question is researched and how the research team will answer the question; second, it includes information on the specific procedures, which medications will be used (if any), which data analysis methods will be used, possible benefits and risks and possible adverse events, and third, it also tells you who can and cannot participate. A protocol also tells you how the research team will protect the health and wellbeing of the participants.

A protocol is a central information source and describes the rules of the clinical trial. First, it states why a specific question is researched and how the research team will answer the question; second, it includes information on the specific procedures, which medications will be used (if any), which data analysis methods will be used, possible benefits and risks and possible adverse events, and third, it also tells you who can and cannot participate. A protocol also tells you how the research team will protect the health and wellbeing of the participants.

A protocol is a central information source and describes the rules of the clinical trial. First, it states why a specific question is researched and how the research team will answer the question; second, it includes information on the specific procedures, which medications will be used (if any), which data analysis methods will be used, possible benefits and risks and possible adverse events, and third, it also tells you who can and cannot participate. A protocol also tells you how the research team will protect the health and wellbeing of the participants.

A protocol is a central information source and describes the rules of the clinical trial. First, it states why a specific question is researched and how the research team will answer the question; second, it includes information on the specific procedures, which medications will be used (if any), which data analysis methods will be used, possible benefits and risks and possible adverse events, and third, it also tells you who can and cannot participate. A protocol also tells you how the research team will protect the health and wellbeing of the participants.

Participating in a clinical trial is 100% your own choice and you should not be forced to participate in a clinical trial. You can also drop out during a clinical trial at any time and should not be forced to continue with the trial if you don’t want to.

Usually, only blinded trials use a placebo, which is an inactive drug or treatment, sometimes also referred to as a “sugar pill”. If you take the placebo, you are in the control group and the goal behind that is to see how the researched drug or treatment compares to the placebo.

Usually, only blinded trials use a placebo, which is an inactive drug or treatment, sometimes also referred to as a “sugar pill”. If you take the placebo, you are in the control group and the goal behind that is to see how the researched drug or treatment compares to the placebo.

Usually, only blinded trials use a placebo, which is an inactive drug or treatment, sometimes also referred to as a “sugar pill”. If you take the placebo, you are in the control group and the goal behind that is to see how the researched drug or treatment compares to the placebo.

Dementia is the general term, or umbrella term, that describes a group of symptoms, for example cognitive decline. Alzheimer’s is a specific and the most common form of dementia: around 60-80% of people who live with dementia live with Alzheimer’s. Nevertheless, also issues other than Alzheimer’s can cause dementia. Important to note is that Alzheimer’s is a progressive disease and can’t be reversed. Some forms of dementia, such as dementia due to vitamin deficiency or drug abuse can be reversible.

Usually, only blinded trials use a placebo, which is an inactive drug or treatment, sometimes also referred to as a “sugar pill”. If you take the placebo, you are in the control group and the goal behind that is to see how the researched drug or treatment compares to the placebo.

Usually, only blinded trials use a placebo, which is an inactive drug or treatment, sometimes also referred to as a “sugar pill”. If you take the placebo, you are in the control group and the goal behind that is to see how the researched drug or treatment compares to the placebo.

Usually, only blinded trials use a placebo, which is an inactive drug or treatment, sometimes also referred to as a “sugar pill”. If you take the placebo, you are in the control group and the goal behind that is to see how the researched drug or treatment compares to the placebo.

Usually, only blinded trials use a placebo, which is an inactive drug or treatment, sometimes also referred to as a “sugar pill”. If you take the placebo, you are in the control group and the goal behind that is to see how the researched drug or treatment compares to the placebo.

Usually, only blinded trials use a placebo, which is an inactive drug or treatment, sometimes also referred to as a “sugar pill”. If you take the placebo, you are in the control group and the goal behind that is to see how the researched drug or treatment compares to the placebo.

Benefits and risks differ from trial to trial and you should always talk to the research team before you decide to participate in a clinical trial to fully understand specific benefits and risks.

Generally, clinical trials may give you access to the best possible treatment for your specific health condition that would otherwise not be available to you. You will also receive attention from a care team consisting of nurses, doctors, and other medical staff, that you would otherwise not get. And, you will help not only research to improve or even find new treatments but as a result, you will also help millions of other people who may be benefitting from these (often live-saving) new treatments in the future as well.

General risks always include possible side effects - that sometimes even need medical attention. If you are part of a randomized trial, this could also mean that there is a placebo (inactive treatment) involved and you could actually get the placebo instead of the real treatment. Or, the trial simply expects too much time commitment from your side.

Usually, only blinded trials use a placebo, which is an inactive drug or treatment, sometimes also referred to as a “sugar pill”. If you take the placebo, you are in the control group and the goal behind that is to see how the researched drug or treatment compares to the placebo.

If you’re thinking of taking part in a clinical trial, you will likely come across an informed consent form. The informed consent form gives you all the information about the purpose of the clinical trial, benefits and potential risks, which procedures are involved in the trial, your rights and that taking part in research is absolutely your choice. It will help you to better understand what to expect when you participate in this specific trial.

A protocol is a central information source and describes the rules of the clinical trial. First, it states why a specific question is researched and how the research team will answer the question; second, it includes information on the specific procedures, which medications will be used (if any), which data analysis methods will be used, possible benefits and risks and possible adverse events, and third, it also tells you who can and cannot participate. A protocol also tells you how the research team will protect the health and wellbeing of the participants.

Huntington’s Disease is a neurodegenerative disorder which affects your body’s nervous system – the network of nerve tissues in the brain and spinal cord that coordinate your body’s activities. It is inherited through a faulty gene, and can cause changes with movement, learning, thinking and emotions. Huntington’s disease affects men and women. It usually develops between the ages of 30 and 50, but can start at any age. Currently, there is no cure, however there is a range options available to ease the effects of the disease. For example, it is important to make any adjustments at home, such as the installation of bannisters and rails, to help mobility. Eating well and staying mentally active are also important steps to take to maintain your quality of life; health professionals and resources from your doctor can help you on your way to making these adaptations.

If you’re thinking of taking part in a clinical trial, you will likely come across an informed consent form. The informed consent form gives you all the information about the purpose of the clinical trial, benefits and potential risks, which procedures are involved in the trial, your rights and that taking part in research is absolutely your choice. It will help you to better understand what to expect when you participate in this specific trial.

When you express interest in participating in a clinical trial, you have to undergo a screening process in order to determine if you actually qualify to participate in the trial. There is a protocol that sets the rules around who can and who cannot participate.

First, you will undergo a pre-screening that usually happens via phone. Here, the trial staff will ask you specific questions about your demographic information and medical history. They will also provide you with more information on the trial. If the clinical trial staff determined that you meet the criteria that are set by the protocol, you will be invited for an on-site screening visit.

At the on-site screening visit, you will go to the clinical trial location (usually in your area). The clinical trial staff will again give you more information on the trial and a qualified doctor will usually perform a physical examination as well and review your medical history.

If you’re thinking of taking part in a clinical trial, you will likely come across an informed consent form. The informed consent form gives you all the information about the purpose of the clinical trial, benefits and potential risks, which procedures are involved in the trial, your rights and that taking part in research is absolutely your choice. It will help you to better understand what to expect when you participate in this specific trial.

If you’re thinking of taking part in a clinical trial, you will likely come across an informed consent form. The informed consent form gives you all the information about the purpose of the clinical trial, benefits and potential risks, which procedures are involved in the trial, your rights and that taking part in research is absolutely your choice. It will help you to better understand what to expect when you participate in this specific trial.

If you’re thinking of taking part in a clinical trial, you will likely come across an informed consent form. The informed consent form gives you all the information about the purpose of the clinical trial, benefits and potential risks, which procedures are involved in the trial, your rights and that taking part in research is absolutely your choice. It will help you to better understand what to expect when you participate in this specific trial.

If you’re thinking of taking part in a clinical trial, you will likely come across an informed consent form. The informed consent form gives you all the information about the purpose of the clinical trial, benefits and potential risks, which procedures are involved in the trial, your rights and that taking part in research is absolutely your choice. It will help you to better understand what to expect when you participate in this specific trial.

A clinical trial helps researchers to understand if a new drug, a new combination of drugs, surgical procedure, medical device, diagnostic method, prevention method or other treatment is effective for a specific health condition, and is safe to use.

If you’re thinking of taking part in a clinical trial, you will likely come across an informed consent form. The informed consent form gives you all the information about the purpose of the clinical trial, benefits and potential risks, which procedures are involved in the trial, your rights and that taking part in research is absolutely your choice. It will help you to better understand what to expect when you participate in this specific trial.

If you’re thinking of taking part in a clinical trial, you will likely come across an informed consent form. The informed consent form gives you all the information about the purpose of the clinical trial, benefits and potential risks, which procedures are involved in the trial, your rights and that taking part in research is absolutely your choice. It will help you to better understand what to expect when you participate in this specific trial.

If you’re thinking of taking part in a clinical trial, you will likely come across an informed consent form. The informed consent form gives you all the information about the purpose of the clinical trial, benefits and potential risks, which procedures are involved in the trial, your rights and that taking part in research is absolutely your choice. It will help you to better understand what to expect when you participate in this specific trial.

If you’re thinking of taking part in a clinical trial, you will likely come across an informed consent form. The informed consent form gives you all the information about the purpose of the clinical trial, benefits and potential risks, which procedures are involved in the trial, your rights and that taking part in research is absolutely your choice. It will help you to better understand what to expect when you participate in this specific trial.

Creutzfeldt-Jakob disease, or CJD, is a rare degenerative disorder which causes rapid damage to the brain’s tissue. Once this damage starts, it continues at a rapid pace and is fatal.

Symptoms of CJD include loss of memory, loss of coordination, changes in personality and slurred speech. Due to the rapid shutdown of the body’s mobility, sufferers are more susceptible to infection and most people diagnosed with CJD die within a year of diagnosis.

There is no cure for CJD, and infections which arise as a result of the disease are not treatable, as the disease is caused by infectious proteins called prions, which remain unaffected by radiation and antibiotics. Hence, the rapid progression of Creutzfeldt-Jakob disease. Once diagnosed, it is helpful to devise a treatment plan in the event that the patient cannot make decisions about their care in the late stage.

When you express interest in participating in a clinical trial, you have to undergo a screening process in order to determine if you actually qualify to participate in the trial. There is a protocol that sets the rules around who can and who cannot participate.

First, you will undergo a pre-screening that usually happens via phone. Here, the trial staff will ask you specific questions about your demographic information and medical history. They will also provide you with more information on the trial. If the clinical trial staff determined that you meet the criteria that are set by the protocol, you will be invited for an on-site screening visit.

At the on-site screening visit, you will go to the clinical trial location (usually in your area). The clinical trial staff will again give you more information on the trial and a qualified doctor will usually perform a physical examination as well and review your medical history.

When you express interest in participating in a clinical trial, you have to undergo a screening process in order to determine if you actually qualify to participate in the trial. There is a protocol that sets the rules around who can and who cannot participate.

First, you will undergo a pre-screening that usually happens via phone. Here, the trial staff will ask you specific questions about your demographic information and medical history. They will also provide you with more information on the trial. If the clinical trial staff determined that you meet the criteria that are set by the protocol, you will be invited for an on-site screening visit.

At the on-site screening visit, you will go to the clinical trial location (usually in your area). The clinical trial staff will again give you more information on the trial and a qualified doctor will usually perform a physical examination as well and review your medical history.

Usually, only blinded trials use a placebo, which is an inactive drug or treatment, sometimes also referred to as a “sugar pill”. If you take the placebo, you are in the control group and the goal behind that is to see how the researched drug or treatment compares to the placebo.

When you express interest in participating in a clinical trial, you have to undergo a screening process in order to determine if you actually qualify to participate in the trial. There is a protocol that sets the rules around who can and who cannot participate.

First, you will undergo a pre-screening that usually happens via phone. Here, the trial staff will ask you specific questions about your demographic information and medical history. They will also provide you with more information on the trial. If the clinical trial staff determined that you meet the criteria that are set by the protocol, you will be invited for an on-site screening visit.

At the on-site screening visit, you will go to the clinical trial location (usually in your area). The clinical trial staff will again give you more information on the trial and a qualified doctor will usually perform a physical examination as well and review your medical history.

When you express interest in participating in a clinical trial, you have to undergo a screening process in order to determine if you actually qualify to participate in the trial. There is a protocol that sets the rules around who can and who cannot participate.

First, you will undergo a pre-screening that usually happens via phone. Here, the trial staff will ask you specific questions about your demographic information and medical history. They will also provide you with more information on the trial. If the clinical trial staff determined that you meet the criteria that are set by the protocol, you will be invited for an on-site screening visit.

At the on-site screening visit, you will go to the clinical trial location (usually in your area). The clinical trial staff will again give you more information on the trial and a qualified doctor will usually perform a physical examination as well and review your medical history.

Clinical trials are so important because they’re the only way to see if new drugs, new combinations of drugs, new treatment methods, medical innovations, diagnostic methods or medical devices actually work for a specific health condition and are safe to use. Without clinical trials, there are no advancements in medicine.

The FDA (Food and Drug Administration) regulates clinical trials and demands that clinical trials must be conducted before a new drug, medical device diagnostic methods or other treatments can be marketed in the United States.

When you express interest in participating in a clinical trial, you have to undergo a screening process in order to determine if you actually qualify to participate in the trial. There is a protocol that sets the rules around who can and who cannot participate.

First, you will undergo a pre-screening that usually happens via phone. Here, the trial staff will ask you specific questions about your demographic information and medical history. They will also provide you with more information on the trial. If the clinical trial staff determined that you meet the criteria that are set by the protocol, you will be invited for an on-site screening visit.

At the on-site screening visit, you will go to the clinical trial location (usually in your area). The clinical trial staff will again give you more information on the trial and a qualified doctor will usually perform a physical examination as well and review your medical history.

When you express interest in participating in a clinical trial, you have to undergo a screening process in order to determine if you actually qualify to participate in the trial. There is a protocol that sets the rules around who can and who cannot participate.

First, you will undergo a pre-screening that usually happens via phone. Here, the trial staff will ask you specific questions about your demographic information and medical history. They will also provide you with more information on the trial. If the clinical trial staff determined that you meet the criteria that are set by the protocol, you will be invited for an on-site screening visit.

At the on-site screening visit, you will go to the clinical trial location (usually in your area). The clinical trial staff will again give you more information on the trial and a qualified doctor will usually perform a physical examination as well and review your medical history.

When you express interest in participating in a clinical trial, you have to undergo a screening process in order to determine if you actually qualify to participate in the trial. There is a protocol that sets the rules around who can and who cannot participate.

First, you will undergo a pre-screening that usually happens via phone. Here, the trial staff will ask you specific questions about your demographic information and medical history. They will also provide you with more information on the trial. If the clinical trial staff determined that you meet the criteria that are set by the protocol, you will be invited for an on-site screening visit.

At the on-site screening visit, you will go to the clinical trial location (usually in your area). The clinical trial staff will again give you more information on the trial and a qualified doctor will usually perform a physical examination as well and review your medical history.

When you express interest in participating in a clinical trial, you have to undergo a screening process in order to determine if you actually qualify to participate in the trial. There is a protocol that sets the rules around who can and who cannot participate.

First, you will undergo a pre-screening that usually happens via phone. Here, the trial staff will ask you specific questions about your demographic information and medical history. They will also provide you with more information on the trial. If the clinical trial staff determined that you meet the criteria that are set by the protocol, you will be invited for an on-site screening visit.

At the on-site screening visit, you will go to the clinical trial location (usually in your area). The clinical trial staff will again give you more information on the trial and a qualified doctor will usually perform a physical examination as well and review your medical history.

When you express interest in participating in a clinical trial, you have to undergo a screening process in order to determine if you actually qualify to participate in the trial. There is a protocol that sets the rules around who can and who cannot participate.

First, you will undergo a pre-screening that usually happens via phone. Here, the trial staff will ask you specific questions about your demographic information and medical history. They will also provide you with more information on the trial. If the clinical trial staff determined that you meet the criteria that are set by the protocol, you will be invited for an on-site screening visit.

At the on-site screening visit, you will go to the clinical trial location (usually in your area). The clinical trial staff will again give you more information on the trial and a qualified doctor will usually perform a physical examination as well and review your medical history.

How long a clinical trial lasts depends on the protocol. It usually lasts from six months to 24 months, but can also last shorter or longer. We encourage you to ask this question to the research staff.

How long a clinical trial lasts depends on the protocol. It usually lasts from six months to 24 months, but can also last shorter or longer. We encourage you to ask this question to the research staff.

Mixed Dementia is the name given to the occurrence of two different forms of dementia which are present in the brain simultaneously. For example, it is not uncommon to see people with both Alzheimer’s Disease and Vascular Dementia present at the same time. The ‘tangles’ of proteins in the brain associated with Alzheimer’s can coexist with the blood vessel changes/blockages associated with Vascular Dementia, and so Mixed Dementia arises. Symptoms can vary depending on which combination of dementia forms the patient has, as well as which parts of the brain are affected. In many cases, symptoms may be similar to (or even indistinguishable from) those of Alzheimer’s.

Currently, there aren’t any pharmaceutical drugs available specifically targeted to treating mixed dementia. If Alzheimer’s disease is diagnosed among the conditions contributing to a person’s dementia symptoms, a doctor may prescribe the medications intended for Alzheimer’s disease treatment.

How long a clinical trial lasts depends on the protocol. It usually lasts from six months to 24 months, but can also last shorter or longer. We encourage you to ask this question to the research staff.

If you wish to volunteer in a clinical trial, you agree to participate and test new drugs, new treatment methods, new diagnostic methods or new medical devices, for example. Important: nobody can force you to participate in a clinical trial and you can drop out at any time, even when you’re already enrolled in a clinical trial.

You should consider the following questions when thinking about joining a clinical trial:

Will the research help me?

What are the risks involved?