Otoferlin-related Auditory Synaptopathy research hub
3 indexed studies · 3 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.
Germany - not yet recruitingNA
Speech-Evoked Auditory Potentials: Multisite Pediatric Evaluation
This study looks at how a new device measures brain responses to speech in babies with and without hearing loss. We want to see how well it works and if it can tell the difference in brain activity when babies use hearing aids.
Australia · Canada - 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.
Germany