Are there any special considerations regarding the health risks of participating in clinical trials?

Yes, there are special considerations regarding the health risks of participating in clinical trials in South Carolina. Clinical trials involve testing the safety and effectiveness of new drugs or treatments on people. Research volunteers should understand that the purpose of the study is not to treat a medical problem but to test a new drug or treatment. Clinical trials come with some risks. Since the treatment or drug is not fully tested, researchers do not yet know the full effects. In addition, participants may be exposed to unknown risks, including medication errors or reactions. It is important to understand the potential risks before participating in a clinical trial. The South Carolina Department of Health and Environmental Control provides a list of important considerations for those considering participating in a clinical trial. These include: informing potential participants of the risks and benefits of participating; providing a clear explanation of the proposed research; and having an informed consent document that includes the potential risks. Participants are also encouraged to ask questions and clarify any concerns before signing the informed consent document. In clinical trials, the well-being of participants is a priority. South Carolina research teams are committed to providing informed consent, closely monitoring participants, and encouraging them to ask questions. If someone wants to participate in a clinical trial, they should take the time to understand the risks and benefits.

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Are there any special considerations regarding the health risks of participating in clinical trials?

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