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Post: Clinical Trials Overview

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Clinical Trials Overview
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UC San Francisco is committed to finding new ways to prevent and treat disease in people, and these efforts involve a form of research called clinical trials.

After a proposed treatment, drug therapy or device is found to be helpful and safe in animals in laboratories, it must also prove to be safe and effective in humans. This evaluation period is known as a clinical trial. A clinical trial also can study human behavior.

As a leading health sciences university, UCSF is actively involved in more than 1,700 clinical trials. All trials are conducted in coordination with UCSF Medical Center, which serves as UCSF’s academic medical center and is consistently ranked among the nation’s top hospitals by U.S. News & World Report . Empowering Patients

To review a list of clinical trials available at UCSF, use our Clinical Trials finder . For a summary of clinical trials throughout the United States and the world that is maintained by the National Institutes of Health (NIH), see NIH Clinical Trials . Find a UCSF Clinical Trial

Browse available trials or search by topic area in a custom tool that collects data from UCSF, ClinicalTrials.gov and other sources. Learn More While clinical trials are considered the fastest way to determine if a proposed intervention is safe and effective, they include both potential benefits and risks. A trial participant has the chance to receive a potentially promising treatment that is not available to the general public and to receive care at the nation’s top academic medical centers and research institutes. Broad and diverse participation in a clinical trial also ensures that the treatment, drug or device will be effective for everyone, not just a segment of the population.

However, those participating in clinical trials face the chance that their disease or condition will not improve with the experimental treatment, and they could experience adverse side effects, among other possible drawbacks.

What is most important for patients is knowledge about and access to clinical trials, so they have the opportunity to participate if they choose and can make informed decisions about their health. Rules on Approval and Adherence

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