Recruiting NCT05402813

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

Longitudinal Study of the Natural History of Two Autosomal Recessive Non Syndromic Deafness (DFNB1A and DFNB9) in Children Up to 16 Years of Age

Sponsor: Sensorion

Conditions AUNB1 Congenital Deafness DFNB1A DFNB9 GJB2 Gene Mutation OTOF Gene Mutation Sensorineural Hearing Loss, Bilateral

Interventions Pure Tone Audiometry Assessment Quality of Life Questionnaires

Updated 6 times since 2022 Last updated: Feb 12, 2025 Started: Nov 18, 2022 Primary completion: Nov 18, 2028 Completion: Nov 18, 2028

Listed as NCT05402813, this observational or N/A phase trial focuses on AUNB1 and Congenital Deafness and remains actively recruiting participants. Sponsored by Sensorion, it has been updated 6 times since 2022, reflecting limited change activity. This study adds to the evidence base for this therapeutic area through structured, versioned documentation.

Status Flow

Change History

6 versions recorded

Mar 2025 — Present [monthly]

Recruiting
Sep 2024 — Mar 2025 [monthly]

Recruiting
Jul 2024 — Sep 2024 [monthly]

Recruiting
Oct 2023 — Jul 2024 [monthly]

Recruiting
Dec 2022 — Oct 2023 [monthly]

Recruiting

Status: Not Yet Recruiting → Recruiting

▶ Show 1 earlier version

Jul 2022 — Dec 2022 [monthly]

Not Yet Recruiting

First recorded

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:

Sensorion

Data source: Sensorion

For direct contact, visit the study record on ClinicalTrials.gov .

Study Locations

• Paris, France