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Clinical Trials – Frequently Asked Questions about Clinical Trials

Choosing to participate in a clinical trial is an important personal decision. The following frequently asked questions will provide you with detailed information about clinical trials and medical research. In addition, it is often helpful to talk to your health care provider, family members, or friends about deciding to join a medical research clinical trial. After you have identified some clinical trial options, the next step is to contact the medical study research staff and ask questions about specific clinical trials.

What is a clinical trial?
What is a protocol?
What are clinical trial phases?
What protections are there for people who participate in clinical trials?
What is an Institutional Review Board (IRB)?
What is informed consent?
Who can participate in a clinical trial?
Who sponsors clinical trials?
What happens during a clinical trial?
What is a placebo?
What is a control or control group?
What is a blinded or masked study?
What is a double blind study?
What are side effects and adverse reactions?
What are the benefits associated with clinical trials?
What are the risks associated with clinical trials?
What should I know before I join a clinical trial?
How should I prepare for a meeting with a research coordinator or doctor?
What questions should I ask?
Should I continue working with my primary health care provider if I participate in a trial?
Can I leave a clinical trial after it has begun?
Will I be paid for participating in a clinical trial?

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