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Otoferlin Patient Registry and Natural History Study

Recruitingn/aAges any - anyAllTobias Moser
NCT05946057 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

This registry is designed to collect comprehensive information about the molecular genetic diagnoses of individuals with otoferlin-associated hearing impairment and clinical information to support a natural history study.

Sign in to get the eligibility rules as simple questions to take to your doctor.

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📋 Eligibility rules (as published)
Inclusion Criteria: * A molecular genetic diagnosis involving biallelic variants in otoferlin (OTOF) and audiometry Exclusion Criteria: * Patients with evidence of non-OTOF molecular genetic diagnoses
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What it tests

  • Molecular genetic testing and audiometry
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Where

1 site
University Medical Center Goettingen
Goettigen, Germany
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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