Frequently Asked Questions
What is a clinical trial?
A clinical trial is a scientific evaluation of the safety and effectiveness of a
new medical treatment, medication or device in human volunteers. Some of the medication
and devices being studied are investigational (not available on the market) and
are being tested for safety and effectiveness. Other medications and devices are
currently available by prescription or over-the-counter and may be tested for a
new dosage or combination with another medication. Clinical trials mostly take place
before new treatments can be available to the public for prescription or over-the-counter.
Why are clinical trials important?
It is important to ensure that after a drug or device is marketed it is safe and
effective treatment for health conditions.
What are the risks of participating in a clinical trial?
Every effort is made to determine the risks during pre-clinical and early clinical
studies. There may be side effects and other health risks that are as of yet unknown.
The reasonably foreseeable risks of a study are listed in the informed consent.
What are the benefits of participating in a clinical trial?
People participate for various reasons, including health, financial, and personal
needs. You can gain valuable information about your medical condition which may
lead to better management of your health. You may also find that the study medication
that you are taking may be helpful with your symptoms.
What are the costs?
There is never a charge for participating in a clinical trial. Study medication,
medical care, and laboratory care is provided at no charge to you or your insurance
company. Qualified participants can possibly be paid for their time and travel.
How do I participate?
If you are interested in one of our studies or would like to inquire about upcoming
studies, please visit our Study Trial Information section of our website or you
can call (706) 243-3669.