Natural History in Children up to 16 Years With Mild to Profound Hearing Loss Due to Mutations in GJB2 / OTOF Genes

Clinical trial NCT05402813 · RECRUITING

Trial details

NCT number: NCT05402813
Sponsor: Sensorion
Status: RECRUITING
Study type: OBSERVATIONAL

Sensorineural Hearing Loss, Bilateral AUNB1 DFNB1A Congenital Deafness DFNB9 OTOF Gene Mutation GJB2 Gene Mutation

Start date: 2022-11-18
Primary completion: 2031-06-01
Enrollment: 180

View on ClinicalTrials.gov

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