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RECRUITING
NCT06680934
CABP2 Patient Registry and Natural History Study
Sponsor: University Medical Center Goettingen
View on ClinicalTrials.gov
Summary
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.
Official title: Patient Registry for Individuals With CABP2-Associated Hearing Loss
Key Details
Gender
All
Age Range
Any - Any
Study Type
OBSERVATIONAL
Enrollment
100
Start Date
2024-08-16
Completion Date
2049-08-16
Last Updated
2026-01-27
Healthy Volunteers
No
Interventions
DIAGNOSTIC_TEST
Molecular genetic testing and audiometry
Genetic testing and audiometry are the interventions of interest
Locations (1)
University Medical Center Goettingen
Göttingen, Germany