CABP2 Patient Registry and Natural History Study

Recruiting Observational Study
CABP2-related Auditory Synaptopathy Hearing Impairment
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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Review the details below, then apply to join this clinical trial.

At a Glance
Sex
Any
Study type
Observational
Participants needed
100 (estimated)
Sponsor
University Medical Center Goettingen · Other
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About This Trial

This registry is designed to collect comprehensive information about the molecular genetic diagnoses and clinical information of individuals with CABP2-associated hearing impairment to support a natural history study.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * A molecular genetic diagnosis involving biallelic variants in CAPB2 and audiometry Exclusion Criteria: * Patients with evidence of non-CABP2 molecular genetic diagnoses
Contacts

Barbara Vona, PhD

+49-551-38-51337

barbara.vona@med.uni-goettingen.de

CONTACT

Tobias Moser, MD

+49-551-39-63070

tmoser@gwdg.de

CONTACT