Unformatted text preview: continuing process throughout the study to provide information for participants. To help someone decide whether or not to participate, the doctors and nurses involved in the trial explain the details of the study. Then the research team provides an informed consent document that includes details about the study, such as its purpose, duration, required procedures, and key contacts. Risks and potential benefits are explained in the informed consent document. The participant then decides whether or not to sign the document. 11/19/07 ME 128 22 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" Those that disallow someone from participating are called "exclusion criteria&quo...
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- Fall '08
- Clinical trial, Clinical Trials Patient Protection Phases, Human Clinical Studies, Cancer Clinical Trials Education Series