Clinical Research Trials

The advancement of science through research.

As a dedicated clinical trial hub, we believe in advancing science through research. We understand each study has the potential of providing treatment for various diseases and disorders. We keep up with the literature and believe in keeping our patients informed.

Our services are closely coordinated with patients, families, sponsors, and regulatory organizations to obtain solid data with strong enrollment in our trials, ensuring high-quality and on-time services. Most importantly, we take excellent care of our patients, ensuring this is a good experience.

FDA-approved Clinical trials are conducted according to a protocol designed by the sponsor and monitored by the IRB. The protocol describes what type of patients may enter the study, schedules of visits, labs, and other procedures, drugs, length of study, and the data/outcomes that will be measured. Each person participating in the study must provide consent before participating. We will clearly outline the study design, help you arrange your appointments, and describe step by step what you can expect when you join a clinical trial.

If you are interested in learning more about our research and finding a clinical trial that best fits you, please get in touch with us to help you throughout the process of evaluation, enrolling, and participating in a research study.