Home › Sensorineural Hearing Loss › NCT06354010

Cross-sectional and Prospective Study to Characterize Early-onset Presbycusis

Who can join

Ages 30 to 55 · All sexes

Inclusion Criteria:

1. Female or Male patients ≥30 and ≤55 years old
2. Bilateral hearing loss first noticed after the age of 16 years old
3. Documented genotyping results showing mutations in GJB2 gene.

Exclusion Criteria:

1. Deafness with a known, non-genetic cause
2. To the opinion of the investigator, unable and/or unwilling to comply with all the protocol requirements and/or study procedures

About the study

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.

What is being tested

• Genotyping (genetic)
• Audiological assessments (other)

Sponsor: Sensorion · Participants: 100 · Started: Jun 14, 2024

Contact the study team

• Lionel HOVSEPIAN, MD · Phone: +33786311376

Official record on ClinicalTrials.gov — NCT06354010

Locations in the U.S.

Conditions

• Sensorineural Hearing Loss
• Presbycusis
• Hearing Disorders and Deafness

From ClinicalTrials.gov, data retrieved Oct 2, 2026. Each study sets its own eligibility; the study team decides who can join.