New registry launched to track rare genetic hearing loss
NCT ID NCT06680934
First seen Jan 29, 2026 · Last updated May 21, 2026 · Updated 23 times
Summary
This study creates a registry for up to 100 people with hearing loss due to changes in the CABP2 gene. Researchers will collect hearing test results and genetic information to better understand how the condition progresses over time. The goal is to gather knowledge that could support future treatments, but no new treatment is being tested.
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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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Locations
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University Medical Center Goettingen
RECRUITINGGöttingen, 37075, Germany
Contact Phone: •••-•••-•••• Email: •••••@•••••
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Conditions
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