Registry for patients with CABP2-related hearing impairment

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This registry collects detailed information about individuals diagnosed with hearing impairment due to CABP2 gene variants. It aims to gather molecular genetic data and clinical information to support a natural history study of this condition. The study is conducted in both German and English and adheres to ethical guidelines approved by the University Medical Center Goettingen's Ethics Committee.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* A molecular genetic diagnosis involving biallelic variants in CAPB2 and audiometry

Exclusion Criteria:

* Patients with evidence of non-CABP2 molecular genetic diagnoses

Where it's running

• University Medical Center Goettingen
  Göttingen, Germany Recruiting

Study contacts

• Principal investigator: Bernd Wollnik, MD — University Medical Center Goettingen
• Study coordinator: Barbara Vona, PhD
• Email: barbara.vona@med.uni-goettingen.de
• Phone: +49-551-38-51337

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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• Evaluating a noise reduction algorithm for cochlear implant users

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.