New study tracks genetic hearing loss in kids to unlock future treatments
NCT ID NCT05402813
First seen Apr 17, 2026 · Last updated May 09, 2026 · Updated 4 times
Summary
This study follows up to 180 children with hearing loss caused by mutations in the GJB2 or OTOF genes. Researchers will measure hearing and brain responses over time to understand how the condition naturally changes. No treatment is given; the goal is to gather information that could help design future therapies.
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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
Email: •••••@•••••
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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Necker Hospital
RECRUITINGParis, France
Conditions
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