Scientists track vision loss in rare eye disease
NCT ID NCT07425574
Summary
This study aims to understand how vision changes over time in people with Stargardt disease and similar inherited eye conditions that cause central vision loss. Researchers will observe 90 participants for up to 2 years, tracking their vision with standard eye tests every 6 months. The goal is to learn if different genetic causes lead to similar patterns of disease progression, which could help design future treatments.
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