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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?

 
   

Who can participate in a clinical trial?

All clinical trials have guidelines about who can participate. Using inclusion/exclusion criteria is an important principle of medical research that helps to produce reliable results. The factors that allow someone to participate in a clinical trial are called "inclusion criteria" and those that disallow someone from participating are called "exclusion criteria". These criteria are based on such factors as age, gender, the type and stage of a disease, previous treatment history, and other medical conditions. Before joining a clinical trial, a participant must qualify for the study. Some research studies seek participants with illnesses or conditions to be studied in the clinical trial, while others need healthy participants. It is important to note that inclusion and exclusion criteria are not used to reject people personally. Instead, the criteria are used to identify appropriate participants and keep them safe. The criteria help ensure that researchers will be able to answer the questions they plan to study.

 
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