RecruitingNCT06354010
Cross-sectional and Prospective Study to Characterize Early-onset Presbycusis
Sponsor
Sensorion
Enrollment
100 participants
Start Date
Jun 14, 2024
Study Type
OBSERVATIONAL
Conditions
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.
Eligibility
Min Age: 30 YearsMax Age: 55 Years
Inclusion Criteria3
- 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.
Exclusion Criteria2
- 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
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Interventions
GENETICGenotyping
Genotyping to determine if patients present mutations to the gene GJB2.
OTHERAudiological assessments
Audiological assessments
Locations(2)
View Full Details on ClinicalTrials.gov
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NCT06354010
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