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

NCT06354010 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2026-05-08

No results posted yet for this study

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.

Conditions

  • Sensorineural Hearing Loss, Bilateral

Interventions

GENETIC

Genotyping

Genotyping to determine if patients present mutations to the gene GJB2.

OTHER

Audiological assessments

Audiological assessments

Sponsors & Collaborators

  • Sensorion

    lead INDUSTRY

Principal Investigators

  • Maya ELZIERE, MD · Hôpital Eureopéen Marseille

Eligibility

Min Age
30 Years
Max Age
55 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-06-14
Primary Completion
2027-07-31
Completion
2027-07-31

Countries

  • United States
  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06354010 on ClinicalTrials.gov