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Participating in Clinical
Trials
Informed Consent
Informed consent is a continuing process that helps you decide
whether to enroll in a trial. During the first meeting and in
follow-up meetings the research team will tell you about
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tests or treatments that you may get if you are assigned to the
treatment group
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possible risks and benefits of these tests or treatments
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standard tests and treatments available now
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what you need to do, such as take medications at a certain
time.
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