New study sheds light on vision loss in rare genetic brain disorders
NCT ID NCT07019558
First seen Nov 20, 2025 · Last updated May 15, 2026 · Updated 24 times
Summary
This study looks at eye and vision problems in people with spinocerebellar ataxia (SCA), a rare genetic brain disease that affects movement and coordination. Researchers will examine 60 adults with SCA types 1, 2, 3, or 27B using detailed eye tests to see how often vision loss occurs. The goal is to better understand these eye issues, not to test a treatment.
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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: •••••@•••••
Locations
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CHU Montpellier - Hôpital Gui de Chauliac
RECRUITINGMontpellier, Hérault, 34000, France
Conditions
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