Clinical Research Trials

What is a Clinical Trial?

A Clinical Trial is sponsored by a pharmaceutical company evaluating the safety and effectiveness of a new therapy for the treatment of the indicated diagnosed medication condition. The Clinical Trial is intended for otherwise healthy patients who may benefit from participation while collecting valuable information that would be provided to the FDA (Federal Drug Administration) for approval then making it available to everyone.

Why would you want to participate in a Clinical Trial?

Clinical Trials may not be for everyone, but for those patients that just are not seeing improvement in their condition, or do not have the financial means to pay for care, this may be an option. ​

Gain access to promising drugs long before they are available to the public.

Aid in research that will contribute to improvements in the field of medicine. 

Individual quality care from experienced Doctors, Nurses, and Clinical Research Coordinators.

The comfort in knowing that all studies are in complete compliance with the Food and Drug Administration (FDA). No cost participation. Our studies and related assessments are free of charge. 

Financial compensation for qualfied participants enrolled in specific studies.

Without Clinical Research there would be no new therapies available. Research also provides continued exploration of the condition or disease to further improve diagnostic testing with the hopes of offering patients better treatments for future generations.

Is Clinical Research Safe?

​Clinical Trials are reviewed and require approval of the Institutional Review Board (IRB) for the safety and wellbeing of the patients who participate. The IRB makes sure that patients are protected and informed of all aspects of the trial. In addition, the FDA regulates the researchers conducting the trials with safeguards for the protection of patients.