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What is Participation in a Trial Like?

When you take part in a clinical trial, you receive your treatment in a cancer center, hospital, clinic, and/or doctor’s office.  Doctors, nurses, social workers, and other health professionals may be part of your treatment team.  This team will follow your progress very closely.  You may have more tests and doctors visits than you would if you were not taking part in a study.  You will follow a treatment plan your doctor prescribes, as specified by the trial protocol, and you may have other responsibilities such as keeping a log or filling out forms about your health.  Some studies continue to check on patients even after their treatment is complete. 

Why are clinical trials important?

There are several reasons why clinical trials are important.  Many experts believe that clinical trials represent the highest quality of care.  The participant may have a positive response to the study medication, and their disease or condition may improve.  In addition, participants may receive free laboratory and medical testing. 

 

Participation in a clinical trial helps manufacturers make informed decisions about whether to pursue bringing a particular drug for approval by the Food & Drug Administration (FDA).  Data from one patient (who completes the entire study) can be an important part of a drug development program.  In the best case scenarios, these data can help get an exciting new drug approved by the FDA, and ultimately, continue the industry’s efforts in developing medications that are safer, more effective, and work faster than any before them.

 

 

Donate to SARC to aid in the search for a cure.

 

 

Find out how SARC is working to find more effective treatments for patients with sarcoma. 

 
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