CABP2 Patient Registry and Natural History Study

Recruiting now

Conditions studied: CABP2-related Auditory Synaptopathy, Hearing Impairment

In brief

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.

Key facts

Study ID

NCT06680934

Run by

University Medical Center Goettingen

People needed

100

Starts

2024-08-16

Expected to finish

2049-08-16

Last updated by the study team

2026-01-27

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

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

You may not qualify if…

• Patients with evidence of non-CABP2 molecular genetic diagnoses

Where it is running

• University Medical Center Goettingen — Göttingen, Germany (enrolling)

Full record on ClinicalTrials.gov

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