How to Get Involved

dgd Research has performed over 1500 Phase I-IV research studies in diabetes, hypertension, neuropathy, osteoporosis, cholesterol, obesity, menopause, nephropathy, as well as other endocrine and metabolic disorders.

We conduct clinical trials under the supervision of major pharmaceutical companies in accordance with FDA rules and regulations. Our dedicated research team is comprised of Physicians, Registered Nurses, Nurse Practitioners, Registered Dieticians, and Physician Assistants.

Participating in a dgd Research study is a simple process. First, participants read an informed consent that explains the purpose of the study. The informed consent also describes the procedures that will be performed throughout the study, any associated risks or benefits of the investigational medication, and any financial compensation for time and travel. Participants then visit with a dgd Research Coordinator to determine if they meet the inclusion/exclusion criteria to enroll in the study. Once enrolled, participants begin taking the investigational medication and performing all study-related procedures until they have completed the study.

dgd Research studies benefit each participant by providing highly supervised, one-on-one medical attention from licensed healthcare professionals at no cost. The specialized attention you receive is additional to the care provided by your regular doctor.

To participate in a dgd Research study, please visit the Currently Enrolling Studies section to view opportunities at each facility, or call (210) 615-5555 to speak with a dgd Research recruiter.