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Clinical Trial Summary

The purpose of this study is to characterize and assess the evolution of hearing impairment of patients with adulthood-onset bilateral sensorineural hearing loss carrying mutations on GJB2 gene.


Clinical Trial Description

This study aims to characterize patients with adulthood-onset bilateral sensorineural hearing loss not due to any underlying medical condition (likely due to a genetic cause) and to assess the evolution of hearing impairment of those carrying mutations in GJB2 gene. Patients who present with adulthood-onset bilateral sensorineural hearing loss will be screened for the presence of mutation involved in hearing impairment. Patients with GJB2 mutations will be proposed to continue in a follow-up period. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06354010
Study type Observational
Source Sensorion
Contact Judith LAREDO, PhD
Phone +33(0)663737108
Email judith.laredo@sensorion-pharma.com
Status Not yet recruiting
Phase
Start date May 2024
Completion date July 2027

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