NCT05402813View on ClinicalTrials.gov

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

RecruitingOBSERVATIONAL
Enrollment

180

Participants

Timeline

Start Date

November 18, 2022

Primary Completion Date

November 18, 2028

Study Completion Date

November 18, 2028

Conditions
Sensorineural Hearing Loss, BilateralAUNB1DFNB1ACongenital DeafnessDFNB9OTOF Gene MutationGJB2 Gene Mutation
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

Trial Locations (1)

Unknown

RECRUITING

Necker Hospital, Paris

Sponsors

Lead Sponsor

Sensorion
All Listed Sponsors
lead

Sensorion

INDUSTRY

NCT05402813 - Natural History in Children Up to 16 Years with Mild to Profound Hearing Loss Due to Mutations in GJB2 / OTOF Genes | Biotech Hunter | Biotech Hunter