Actively Recruiting
CABP2 Patient Registry and Natural History Study
Led by University Medical Center Goettingen · Updated on 2026-01-27
100
Participants Needed
1
Research Sites
1304 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
CABP2 Patient Registry and Natural History Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- A molecular genetic diagnosis involving biallelic variants in CABP2 and audiometry
You will not qualify if you...
- Patients with evidence of non-CABP2 molecular genetic diagnoses
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University Medical Center Goettingen
Göttingen, Germany, 37075
Actively Recruiting
Research Team
B
Barbara Vona, PhD
CONTACT
T
Tobias Moser, MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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