We are experts in conducting clinical trials in psychiatry, neurology, and general medicine to help bring advanced pharmacologic treatments to patients and the public.

A clinical trial is a research study conducted by a physician which investigates the effects of a drug, medical treatment, or medical device as part of the research process.

There are a number of reasons for participation in research studies:

• An alternative to current medication
• An opportunity to try medications which may not be available to the general public
• Receive excellent care and are closely monitored by leading physicians and clinical staff
• An opportunity to help current and future generations by testing medications/treatments
• Participation is free
• Participation is voluntary

In exchange for the voluntary participation in our research, we provide professional care, investigational medication, and close monitoring for each of our patients at no cost and there is no need for health insurance. Research participants generally receive monetary compensation for time and travel.

The government has put in place strict guidelines and safequards to protect those who choose to participate in clinical trials.  Every study conducted within the U.S. is approved and monitored by an Institutional Review Board (IRB).  The IRB ensures that a clinical trial is conducted ethically and that the rights of study participants are protected. Your medical status during the study is also closely monitored by a study physician.

• You will be completely informed regarding your involvement and all the risks and benefits will be explained to you
• You will receive a medical/physical examination by a physician and your diagnosis and plan of care will be discussed
• In the beginning of your involvement, you will be in the screening phase, which varies in length of time
• Upon completion of the screen, if you meet all criteria of the study, you may elect to enroll in the study
• Throughout the course of the study, you will meet regularly with the study coordinator and physician
• Your progress will be monitored with the new medication/treatment

Your Privacy:
Goldpoint Clinical Research is committed to patient confidentiality and you may review and receive a copy of our Confidentiality Statement and obtain answers to any questions you may have.

You will be given the medication/treatment being studied based upon your diagnosis.  All of the potential side effects of the drug are thoroughly explained prior to initiation of your treatment.  Should you develop side effects, the physician overseeing your treatment will take all necessary steps to ensure your safety.

In some studies, the medication being studied may be compared to a placebo.  A placebo is an inactive substance that is believed to cause no change in the individual receiving it.  Both you and your physician may not be aware of whether you are receiving a placebo.

Should symptoms worsen, steps will be taken to ensure your safety and level of comfort.