Clinical Research
The clinical research department at Katzen Eye Group was developed to ensure high quality preclinical and clinical trials in vision research. These studies introduce new technology and medication to patients.
Katzen Eye Group research team is made up of a group of board certified ophthalmologists, optometrists and clinical research coordinators. We are also partnered with Rx Trials, an experienced research consulting firm.
Internationally recognized as a team of eye care professionals and researchers, Katzen Eye Group is dedicated to improving the quality of care to patients. Through a commitment of excellence, unrivaled in the eye care industry, our aim is to offer the most advanced treatment in a warm and friendly atmosphere. Our major areas of interest include: dry eyes, age related macular degeneration, diabetic retinopathy, cataracts, glaucoma and contact lenses.
The Importance Of Vision Research
Millions of Americans suffer with vision impairment, which is among the most common disabilities in the U.S. In addition, clinical research is an important avenue for patients to receive promising new therapies that may not otherwise be available. At Katzen Eye Group, we are dedicated to the highest standards of research.
Clinical Research Registry
Understanding Clinical Trials
Choosing to participate in a clinical trial is an important personal decision. The following frequently asked questions provide detailed information about clinical trials. In addition, it is often helpful to talk to a physician, family members, or friends about deciding to join a trial. After identifying some trial options, the next step is to contact the study research staff and ask questions about specific trials.
- What is a clinical trial?
- Why participate in a clinical trial?
- Who can participate in a clinical trial?
- What happens during a clinical trial?
- What is informed consent?
- How is the safety of the participant protected?
- What should people consider before participating in a trial?
- Does a participant continue to work with a primary health care provider while in a trial?
- Can a participant leave a clinical trial after it has begun?
- What is a protocol?





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