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RECRUITING
NCT05402813

Natural History in Children up to 16 Years With Mild to Profound Hearing Loss Due to Mutations in GJB2 / OTOF Genes

Sponsor: Sensorion

View on ClinicalTrials.gov

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

Interventions

OTHER

Pure Tone Audiometry Assessment

Collection of Pure Tone Audiometry data performed in routine practice during study period

OTHER

Quality of Life Questionnaires

Collection of Quality of Life questionnaire's answers during study period

Locations (1)

Necker Hospital

Paris, France