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

NCT05402813 · clinicaltrials.gov ↗

RECRUITING

Status

180

Enrollment

INDUSTRY

Sponsor class

Conditions

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

Interventions

OTHER: Pure Tone Audiometry Assessment
OTHER: Quality of Life Questionnaires

Sponsor

Sensorion