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Introduction to Clinical Trials  I  Glossary  I  General Information on Clinical Trials

Participation In Clinical Trials
For those considering participation in a clinical trial, the following frequently asked questions are important in understanding the role of the participant and the unique process of clinical trials.
»  Who can participate in a clinical trial?
»  What happens during a clinical trial?
»  What is informed consent?
»  What kind of preparation should a potential participant make for
    the meeting with the research coordinator or doctor?
»  What should people consider before participating in a trial?
»  Does a participant continue to work with a primary health care
    provider while in a trial?
»  What are side effects and adverse reactions?
»  What are the benefits and risks of participating in a clinical trial?
»  How is the safety of the participant protected?
»  Can a participant leave a clinical trial after it has begun?

 
   

What happens during a clinical trial?

The clinical trial process depends on the kind of trial being conducted (See What are the different types of clinical trials?) The clinical trial team includes doctors and nurses as well as social workers and other health care professionals. They check the health of the participant at the beginning of the trial, give specific instructions for participating in the trial, monitor the participant carefully during the trial, and stay in touch after the trial is completed.

Some clinical trials involve more tests and doctor visits than the participant would normally have for an illness or condition. For all types of trials, the participant works with a research team. Clinical trial participation is most successful when the protocol is carefully followed and there is frequent contact with the research staff.

 
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