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 Oregon. All participants of clinical trials must be given informed consent before they are enrolled, which includes documentation of any risks associated with the trial and a description of the potential benefits. This includes considering any possible physical, psychological, and financial risks. For example, if the clinical trial involves the use of medication, participants must be informed of any potential side effects as well as the possible health risks of using the medication. Additionally, participants must be aware of any potential costs associated with the clinical trial, such as the cost of prescribed medications or any additional tests or treatments. Participants must also be aware of their rights, such as the right to withdraw from the trial at any time. The Oregon Clinical Trials Registry is a great resource for potential participants to learn more about the risks and benefits associated with participating in clinical trials in Oregon.

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