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Clinical Trial Summary

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 10 years of age.


Clinical Trial Description

The study aims to: - better describe the prevalence of cases of DFNB1A and DFNB9, including the type of mutations, and to assess the clinical course of the disease in children up to 10 years of age who have a moderate to profound deafness. - better understand the audiological and genetic characteristics of the participants with congenital versus evolutive DFNB1A and DFNB9 deafness. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05402813
Study type Observational
Source Sensorion
Contact Judith LAREDO, PhD
Phone +33(0)663737108
Email judith.laredo@sensorion-pharma.com
Status Recruiting
Phase
Start date November 18, 2022
Completion date November 18, 2026

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