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Participation in Clinical Trials  I  Glossary  I  General Information on Clinical Trials

An Introduction to Clinical Trials
Choosing to participate in a clinical trial is an important personal decision. The following frequently asked questions provide introductory information about clinical trials. In addition, it is often helpful to talk to a physician, family members, or friends about deciding to join a trial. After identifying some trial options, the next step is to contact the study research staff and ask questions about specific trials.
»  What is a clinical trial?
»  Why participate in a clinical trial?
»  Where do the ideas for trials come from?
»  Who sponsors clinical trials?
»  What is a protocol?
»  What is a placebo?
»  What is a control or control group?
»  What are the different types of clinical trials?
»  What are the phases of clinical trials?

 
   

What are the phases of clinical trials?

Clinical trials are conducted in phases. The trials at each phase have a different purpose and help scientists answer different questions:

In Phase I trials, researchers test a new drug or treatment in a small group of people (20-80) for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.

In Phase II trials, the study drug or treatment is given to a larger group of people (100-300) to see if it is effective and to further evaluate its safety.

In Phase III trials, the study drug or treatment is given to large groups of people (1,000-3,000) to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.

In Phase IV trials, post marketing studies delineate additional information including the drug's risks, benefits, and optimal use.

 
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