Cross-sectional and Prospective Study to Characterize Early-onset Presbycusis
Recruiting now
Conditions studied: Sensorineural Hearing Loss, Bilateral
In brief
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.
Key facts
- Study ID
- NCT06354010
- Run by
- Sensorion
- People needed
- 100
- Starts
- 2024-06-14
- Expected to finish
- 2027-07-01
- Last updated by the study team
- 2026-05-08
Who can join
Age: 30 and older, up to 55. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Female or Male patients ≥30 and ≤55 years old
- Bilateral hearing loss first noticed after the age of 16 years old
- Documented genotyping results showing mutations in GJB2 gene.
You may not qualify if…
- Deafness with a known, non-genetic cause
- To the opinion of the investigator, unable and/or unwilling to comply with all the protocol requirements and/or study procedures
Where it is running
- The University of South Florida Board of Trustees — Tampa, Florida, United States (enrolling)
- CHU Gui de Chauliac — Montpellier, France (enrolling)
Full record on ClinicalTrials.gov
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