About Clinical Trials

A clinical trial is a study involving human volunteers to assess new techniques for screening, prevention, diagnosis, or treatment of a disease.

A clinical trial serves to assess the safety and effectiveness of an investigational drug or therapy, as well as explore innovative applications for existing treatments. These trials are meticulously planned and supervised to safeguard the well-being of patient volunteers. Prior to the general public’s use, medications must undergo clinical trials mandated by the Food and Drug Administration (FDA).

Study coordinators and physicians diligently observe participants during the study through physical examinations, laboratory tests, and various medical procedures. These processes are commonly viewed as an extension of standard patient care. Patients involved in research studies receive study medication, tests, and examinations free of charge during the study period.

Research can span from weeks to months, or even years, enabling patients to avoid the significant expenses linked to office visits and purchasing medications. Participating in a clinical study is a personal decision, and we aim to equip you with the necessary information for an informed choice. We encourage you to discuss this decision with your loved ones too. If you choose to participate, we ensure that your journey is straightforward and filled with valuable information.