Scientists track rare eye disease over time to pave way for future treatments
NCT ID NCT04591483
Summary
This study aims to understand how a rare, inherited eye disease called Stargardt-like macular dystrophy (STGD3) changes over time. Researchers will follow 25 patients aged 10 and older for three years, using detailed eye exams and imaging to track the disease's natural progression. The goal is to gather essential information to help design future treatments, as there is currently no cure for this condition.
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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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