All treatments
Treatment
Molecular genetic testing and audiometry clinical trials
2 indexed studies · 2 currently recruiting
- Recruiting
Otoferlin Patient Registry and Natural History Study
This study collects information from people with hearing loss caused by a specific gene called otoferlin. Its aim is to better understand this type of hearing loss, which could help develop new treatments in the future.
For: Otoferlin-related Auditory Synaptopathy · Hearing ImpairmentGermany - Recruiting
CABP2 Patient Registry and Natural History Study
This study is gathering information about people in the UK and Germany who have hearing loss caused by changes in a specific gene called CABP2. It aims to understand how this type of hearing loss develops over time. Participants will share their genetic test results and hearing checks to help researchers learn more.
For: CABP2-related Auditory Synaptopathy · Hearing ImpairmentGermany