FAQ about Clinical Research.
Here we provide answers to frequently asked questions Studies.

The Most Asked Questions About Studies.

Q Who is Eligible to Participate?
A These trials are available to our patients, their families and the general public.  You do not have to be a patient at this office to participate in these trials. They are open to all who qualify no matter what type of insurance they have, as participation is free of charge..

Q Is It Safe?
A The FDA and the Institutional Review Board (IRB) approve all study designs. The IRB was developed to protect the rights of all research subjects.  This Board reviews all aspects of the information regarding the study prior to any patient being enrolled.  All patients will receive an informed consent form, prior to entering a study. It describes the study, the requirements of the volunteer, duration of the study and the known side effects of the medication.  Your signed approval is required before starting.

Q Why Participate In Research?
A Participants receive valuable information about their disease and condition, medical tests, health exams and medical advice, free of charge.  Volunteers in clinical research trials make the development of new and better medications possible.  In addition, participants are financially compensated for their time and travel.