The Conrad Pearson Clinic is a leader in clinical research and is unique in that we are the only practice in the region that has such a wide breadth of clinical research offerings. Led by Dr. Paul Eber and Dr. Michael Granieri, our research team offers clinical trials to allow us to remain at the forefront of medicine and to allow our patient access to the newest treatment options.
What is clinical research?
Clinical research is the process through which new treatments, technologies, and approaches to care are developed and tested. A clinical trial is a structured study designed to evaluate the safety and effectiveness of medications, procedures, diagnostics, or therapies. Nearly every advancement in modern medicine, from new cancer treatments to minimally invasive procedures has been made possible through clinical research. At Urology Alliance, we are proud to play a leading role in bringing these advancements forward, with a focus on precision, accuracy, and high-quality data that physicians and patients can trust.
Why participate in a study?
Clinical trials offer meaningful opportunities for patients:
- Access to innovative treatments before they are widely available
- Personalized, closely monitored care from a dedicated research team
- The opportunity to contribute to medical advances that may benefit others
Many studies are designed to improve areas where current treatments fall short. For some patients, participation can provide access to options that better align with their specific condition and goals. Our team is committed to connecting the right patients to the right studies, ensuring that participation is thoughtful, appropriate, and aligned with each individual’s care plan.
Are clinical trials safe?
All medical decisions, including participation in a clinical trial, carry some level of risk. However, patient safety is the foundation of every study we conduct. Clinical trials are performed under multiple layers of oversight. Each study is reviewed by an independent Institutional Review Board (IRB) to ensure patient protection, and many are regulated by the U.S. Food and Drug Administration (FDA). Patients are supported throughout the process by experienced clinical research coordinators and physician investigators who provide attentive, responsive care. Our team is committed to maintaining the highest standards of safety, ethics, and accountability at every step.
The Conrad Pearson Clinical Research Department is currently recruiting participants for clinical trials. Explore our active studies to learn more about eligibility and participation.
For compliance we post our Institutional Biosafety Committee meeting minutes here:
