Scientists track rare eye disease in search for future treatments
NCT ID NCT04591483
Summary
This study aims to understand how a rare inherited eye disease called Stargardt-like macular dystrophy (STDG3) changes over several years. Researchers will observe up to 25 people with a specific genetic mutation, tracking their vision and eye health through regular exams and imaging tests over three years. The goal is to gather detailed information about the disease's natural progression, which is needed to design and test potential future treatments.
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Contacts and locations
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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National Institutes of Health Clinical Center
RECRUITINGBethesda, Maryland, 20892, United States
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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