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Natural History in Children up to 16 Years With Mild to Profound Hearing Loss Due to Mutations in GJB2 / OTOF Genes
Sponsor: Sensorion
Summary
The purpose of this study is to follow the natural history of non-syndromic hearing loss caused by mutations in two genes (GJB2 or OTOF) in children up to 16 years of age.
Official title: Longitudinal Study of the Natural History of Two Autosomal Recessive Non Syndromic Deafness (DFNB1A and DFNB9) in Children up to 16 Years of Age
Key Details
Gender
All
Age Range
Any - 16 Years
Study Type
OBSERVATIONAL
Enrollment
180
Start Date
2022-11-18
Completion Date
2028-11-18
Last Updated
2026-04-06
Healthy Volunteers
No
Conditions
Interventions
Pure Tone Audiometry Assessment
Collection of Pure Tone Audiometry data performed in routine practice during study period
Quality of Life Questionnaires
Collection of Quality of Life questionnaire's answers during study period
Locations (1)
Necker Hospital
Paris, France