A clinical research registry is a secure database where participants’ information—such as demographics, contact details, and medical history—is collected and stored over time to support meaningful research.
The registry’s goal is to build a comprehensive, diverse database of participants at Texas Southern University’s Center for Clinical Research and Translational Sciences (CCRTS). It helps identify individuals for a wide range of clinical studies, from observational research to interventional trials.
By joining, you contribute to advancing medical knowledge, improving treatments, and ensuring diverse representation in clinical research. Both individuals with medical conditions and healthy volunteers are welcome.