Taking peopleNo phase
CABP2 Patient Registry and Natural History Study
This trial has no sites in United States.
It has sites in one country. Choose a country to see its sites.
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record → Contacts and Locations
Print a page for my doctorTrial details
- Who runs it
- University Medical Center Goettingen
- Trial code
- NCT06680934
- Record updated
- 27 January 2026
- Original description
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.Read full original descriptionShow less
Patient Registry for Individuals With CABP2-Associated Hearing Loss
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.
Inclusion: A molecular genetic diagnosis involving biallelic variants in CAPB2 and audiometry.
Exclusion: Patients with evidence of non-CABP2 molecular genetic diagnoses.