New study tracks eye disease in rare Deaf-Blind condition
NCT ID NCT07278843
First seen Jan 05, 2026 · Last updated May 22, 2026 · Updated 23 times
Summary
This study follows 60 people with Usher syndrome type 1B, a rare genetic condition causing deafness and progressive vision loss. Researchers will measure how vision changes over time using standard eye tests and new virtual reality tools. The goal is to better understand the disease and validate tests for future treatment trials. No experimental treatment is given.
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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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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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Centre National d'Ophtalmologie des Quinze-Vingts
RECRUITINGParis, Île-de-France Region, 75012, France
Contact Phone: •••-•••-•••• Email: •••••@•••••
Conditions
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