Status: Recruiting
Natural History in Children up to 16 Years With Mild to Profound Hearing Loss Due to Mutations in GJB2 / OTOF Genes
The purpose of this study is to follow the natural history of non-syndromic hearing loss caused by mutations in two genes (GJB2 or OTOF) in children up to 16 years of age.
Participants needed: 180
Trial details
Age: Up to 16Biological sex: AllType: ObservationalSponsor: SensorionUpdated: Jun 1, 2026Locations: 1
Eligibility criteria
Aged ≤ 16 years on the date of signed informed consent for cohort 1 and ≤ 10 yea... [+4]
Other type of deafness, such as unilateral deafness, persistent conductive deafn... [+2]