Clinical Trials

Clinical trials (also called research studies) are used by researchers to determine whether new drugs or treatments are both safe and more effective than the current standard of treatment. Comprehensive clinical trials are the quickest and most effective way to find treatments that work. Every clinical trial in the U.S. must be approved and monitored by an Institutional Review Board (IRB). The IRB oversees the ethical and physical protection of the people who choose to participant in clinical trials.

Participating in a clinical trial is an important personal decision that should be discussed with your physician and health care provider. There are both gains and risks associated with clinical trials. By participating in a clinical trail you may benefit from new treatments that are not yet available to the public. You will also be actively involved in your own health as well as the health of others by contributing to research.

Before participating in a clinical trial you should also be aware of the risks which may include side affects or adverse reactions to medications or treatments. Depending on the clinical trial you choose to participate in a portion of your time may be required for treatments, hospitals visits, or involved dosage requirements.