Our Research Program
Advancing vision care in West Virginia through discovery, innovation, and patient-centered research.
Retina Consultants of West Virginia is proud to be launching a new, FDA-regulated clinical research program dedicated to advancing the treatment of retinal diseases. While our research program is in its early stages, it is built on a strong foundation of clinical excellence, trusted partnerships, and a shared commitment to improving patient outcomes.
Our goal is to bring innovative therapies and investigational treatments to our patients—providing access to new options that may not yet be available through standard care. As our research program grows, we plan to participate in clinical trials focused on a range of retinal conditions, contributing to the future of vision care while offering hope to patients today.
Through carefully selected trials, we aim to support progress in areas such as emerging therapeutics, novel drug delivery systems, and advanced imaging—always with patient safety and ethics at the forefront.
What Is a Clinical Trial?
A clinical trial is a medical research study designed to evaluate new ways to diagnose, treat, or prevent disease. At Retina Consultants of West Virginia, clinical trials are conducted in partnership with reputable pharmaceutical and biotechnology companies and are overseen by experienced physicians and trained research staff. Every study follows strict FDA regulations and ethical standards and is monitored by independent review boards to ensure participant safety. Clinical trials allow patients to play an important role in advancing medical knowledge while receiving attentive, closely monitored care.
Why Participate in a Clinical Trial at Retina Consultants of WV?
Our clinical research program offers eligible patients access to investigational treatments that go beyond traditional care—within a controlled, closely supervised environment. For some patients, especially those who have not seen the results they hoped for with current treatments, clinical trials may offer new possibilities. Participation also helps advance retinal care for future patients across West Virginia and beyond. As a startup research program, we are intentionally selective, patient-focused, and committed to providing a high level of individualized attention throughout the study process.
Potential Benefits of Participating in a Clinical Trial
Depending on the study, potential benefits may include:
- Early access to investigational treatments not yet available to the public
- Study-related exams, imaging, procedures, and medications provided at no cost
- No insurance required for study-related care
- Possible stipends for completed study visits
- Dedicated support from a research coordinator throughout the study
- Close monitoring by board-certified retina specialists
- The opportunity to contribute to the future of retinal disease treatment
Benefits vary by study, and participation is always voluntary.
Eligibility and Enrollment
Participation in a clinical trial at Retina Consultants of West Virginia typically requires that you are an established patient in our practice. During a routine retinal evaluation, your physician may determine whether you could be a candidate for a current or upcoming study.
Eligibility is based on specific study criteria, which may include:
- Your diagnosis and stage of disease
- Medical history and overall health
- Age
- Current vision level
- Prior or current treatments
Our physicians and research team will carefully review your information to determine whether a study is appropriate and safe for you. If you qualify, we will take time to explain the study in detail, answer your questions, and help you decide whether participation is right for you.
Your Safety Comes First
Patient safety is our top priority. All clinical trials offered through Retina Consultants of West Virginia adhere to strict FDA guidelines and are approved and monitored by independent Institutional Review Boards (IRBs). Some studies may also involve additional safety monitoring committees. Our physicians and research staff closely monitor participants throughout the study with regular exams and testing. Participation is only recommended when a study is medically appropriate and aligned with your best interests. If at any point a study presents unexpected risks, it may be modified, paused, or stopped entirely to protect participants.
Why Choose Retina Consultants of West Virginia for Clinical Research?
- A newly established, patient-focused retinal research program
- Board-certified retina specialists with deep clinical expertise
- Careful selection of FDA-regulated clinical trials
- Advanced diagnostic and imaging technology
- A commitment to expanding access to innovative retinal care in West Virginia