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

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Trial ID: NCTNCT05402813

Status: 🟢 Enrolling Now

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

Phase: Research Study

Find a Study Location Near You

This study is available at 1 research site. We'll help you connect with the location that's right for you.

Participating sites include:

• Paris,

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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 - Join Clinical Trial NCTNCT05402813

How to Join This Clinical Trial - NCTNCT05402813

Learn how to participate in this clinical trial studying an investigational therapy for Sensorineural Hearing Loss, Bilateral, AUNB1, DFNB1A, Congenital Deafness, DFNB9, OTOF Gene Mutation, GJB2 Gene Mutation. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Sensorineural Hearing Loss, Bilateral, AUNB1, DFNB1A, Congenital Deafness, DFNB9, OTOF Gene Mutation, GJB2 Gene Mutation. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied: Sensorineural Hearing Loss, Bilateral, AUNB1, DFNB1A, Congenital Deafness, DFNB9, OTOF Gene Mutation, GJB2 Gene Mutation
Treatment Being Tested: Investigational treatment
Study Phase: Clinical trial phase - Research study
Enrollment Status: Currently enrolling participants
Study Identifier: NCTNCT05402813 - ClinicalTrials.gov Identifier
Sponsored By: Study sponsor

What to Expect as a Participant

Participating in this clinical trial involves:

Initial screening to determine eligibility
Regular study visits and health assessments
Receiving the study treatment or placebo
Medical monitoring and follow-up care
Contributing to medical research that may help others
Potential access to new treatments before they're widely available

Clinical Trial Benefits and Compensation

Participants in this clinical research study may receive:

Close medical monitoring by healthcare professionals
Access to potential new treatments
Compensation for time and travel (varies by study)
No-cost study-related medical care
The opportunity to help advance medical knowledge

Where Is This Clinical Trial Located?

This study is enrolling participants at 1 locations. Find a study site near you:

Clinical Research Site

Paris, - France

Status: RECRUITING

How to Enroll in This Study

To learn more about participating in this clinical trial for Sensorineural Hearing Loss, Bilateral, AUNB1, DFNB1A, Congenital Deafness, DFNB9, OTOF Gene Mutation, GJB2 Gene Mutation:

Review the eligibility criteria with your healthcare provider
Contact the study team for a pre-screening interview
Schedule an in-person screening visit if eligible
Review and sign the informed consent form
Begin participation in the clinical trial

Why Choose Quri.ai as Your Clinical Trial Matching Service

Quri.ai is a free clinical trial matching service that helps patients connect with research sites. We make it easier to:

Find clinical trials that match your condition
Get matched to the right study location near you
Connect directly with study coordinators
Understand if you qualify with simplified eligibility screening
Navigate the enrollment process with personalized support
Access new treatments through clinical research participation