10-Year eye study seeks clues to genetic vision loss
NCT ID NCT01736293
First seen Nov 01, 2025 · Last updated May 01, 2026 · Updated 22 times
Summary
This study follows 68 people aged 12 and older who have ABCA4 gene mutations, which can cause vision loss. Over 10 years, researchers will track how the disease progresses using eye exams, blood tests, and skin samples. No treatment is given; the goal is to gather information for future clinical trials.
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Locations
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National Institutes of Health Clinical Center
Bethesda, Maryland, 20892, United States
Conditions
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