New registry aims to unlock secrets of rare genetic hearing loss
NCT ID NCT06680934
First seen Jan 29, 2026 · Last updated May 16, 2026 · Updated 22 times
Summary
This study is creating a registry for up to 100 people with hearing loss caused by changes in the CABP2 gene. Researchers will collect hearing test results and genetic information to better understand how this condition progresses over time. The goal is to gather knowledge that could support future treatments, but this study does not test any new therapy.
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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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University Medical Center Goettingen
RECRUITINGGöttingen, 37075, Germany
Contact Phone: •••-•••-•••• Email: •••••@•••••
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Contact
Contact
Contact Phone: •••-•••-•••• Email: •••••@•••••
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Conditions
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