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First received: August 21, 2023

Clinical Trial: A Natural History Study in Pediatric Participants With Hearing Loss Due to OTOF, GJB2, or GJB2/GJB6 Mutations

Study Status: Completed

Recruit Status: RECRUITING

Condition: Congenital Hearing Loss Secondary to Biallelic Mutations in the Otoferlin Gene (OTOF)

Study Type: OBSERVATIONAL


Official Title: A Retrospective and Prospective Natural History Study to Examine the Characteristics of Gene-Related Hearing Loss in Pediatric Participants With Biallelic Otoferlin (OTOF) Mutations, Gap Junction Beta

Brief Summary: This is an observational study to examine the characteristics of gene-related hearing loss in pediatric participants with biallelic otoferlin (OTOF) Mutations, Gap Junction Beta 2 (GJB2) Mutations, or Digenic GJB2/Gap Junction Beta 6 (GJB6) Mutations.This study will follow the participant for 4 years with annual visits each year.

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