Global Medical Institutes, LLC

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 are side effects and adverse reactions?

Side effects are any undesired actions or effects of drug or treatment. Negative or adverse effects may include headache, nausea, hair loss, skin irritation, or other physical problems. Experimental treatments must be evaluated for both immediate and long-term side effects.