SCA7 study seeks to unlock secrets of rare brain and eye disease
NCT ID NCT02741440
First seen Nov 01, 2025 · Last updated May 13, 2026 · Updated 25 times
Summary
This study follows people with spinocerebellar ataxia type 7 (SCA7), a genetic disease that causes problems with coordination, balance, speech, and vision. Researchers want to track how the disease progresses over 5 years by doing eye tests, brain scans, and neurological exams. The goal is to learn more about SCA7 to help develop future treatments. Participants must be 12 or older and have a confirmed SCA7 diagnosis.
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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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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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