← Eichor
Condition: Congenital Hearing Loss Synced from ClinicalTrials.gov · July 28, 2026

Recruiting studies: Congenital Hearing Loss

Studies currently listed as recruiting on the public registry for this search term. Each page explains the study in plain language, with locations and the study team's contact details. Clinicians: generate a printable list for your patient →

KHENERFIN Study: A Trial to Evaluate the Efficacy and Safety of Sonlicromanol in Primary Mitochondrial Diseases
Phase 3 · 10 location(s) · Khondrion BV · NCT06451757A Study of EH002 Gene Therapy for Otoferlin Gene Mutation-mediated Hearing Loss
NA · 2 location(s) · Yilai Shu · NCT06722170Overview of Targeted Screening for Congenital Infection Guided by Neonatal Hearing Screening
Phase N/A · 1 location(s) · University Hospital, Strasbourg, France · NCT07335874Natural History of Photoreceptor Degeneration in USH1B: Clinical Parameters and Validation of Functional Vision Tests in
Phase N/A · 1 location(s) · Centre Hospitalier National d'Ophtalmologie des Quinze-Vingt · NCT07278843Natural History in Children up to 16 Years With Mild to Profound Hearing Loss Due to Mutations in GJB2 / OTOF Genes
Phase N/A · 1 location(s) · Sensorion · NCT05402813Pitch Perception and Memory: Deficits and Training
NA · 1 location(s) · Hospices Civils de Lyon · NCT03707691A Comparative Analysis of Speech Perception Between Cochlear Implant Patients and DFNB9 Patients Receiving Gene Therapy
Phase N/A · 6 location(s) · Eye & ENT Hospital of Fudan University · NCT06237790Protein Biomarkers and Host RNA Expression Profiles in Congenital Cytomegalovirus Infection
Phase N/A · 2 location(s) · Rigshospitalet, Denmark · NCT07635368Effects of Bisphosphonates on OI-Related Hearing Loss
Phase 4 · 1 location(s) · Hospital for Special Surgery, New York · NCT04152551Characterization and Contribution of Genome-wide DNA Methylation (DNA Methylation Episignatures) in Rare Diseases With P
Phase N/A · 1 location(s) · Assistance Publique - Hôpitaux de Paris · NCT06475651Audio-vestibular Evaluation of Children and Young Adults With Osteogenesis Imperfecta
Phase N/A · 1 location(s) · Assistance Publique - Hôpitaux de Paris · NCT05419960Perceptual Evaluation and Rehabilitation System Development for Congenital Hearing Loss
NA · 1 location(s) · Eye & ENT Hospital of Fudan University · NCT07024524North American Mitochondrial Disease Consortium Patient Registry and Biorepository (NAMDC)
Phase N/A · 17 location(s) · Columbia University · NCT01694940A Study of DB-OTO, an Adeno-Associated Virus (AAV) Based Gene Therapy, in Children/Infants, Adolescents and Adults With
Phase 1/Phase 2 · 16 location(s) · Regeneron Pharmaceuticals · NCT05788536Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford
Phase N/A · 2 location(s) · Sanford Health · NCT01793168Study of N-acetylcysteine in the Treatment of Patients With the m.3243A>G Mutation and Low Brain Glutathione Levels
Phase 1 · 1 location(s) · Michio Hirano, MD · NCT05241262Genetic and Epigenetic Background of Inner Ear Dysfunction in Turner Syndrome
Phase N/A · 1 location(s) · Gødstrup Hospital · NCT06507007Natural History Study of Usher Syndrome ( Light4Deaf )
Phase N/A · 4 location(s) · Centre Hospitalier National d'Ophtalmologie des Quinze-Vingt · NCT04665726Study of Subretinally Injected AAVB-081 in Patients With Usher Syndrome Type IB (USH1B) Retinitis Pigmentosa
Phase 1/Phase 2 · 3 location(s) · AAVantgarde Bio Srl · NCT06591793Analysis of Parental Support in Families Using the LENA After Early Cochlear Implantation
Phase N/A · 1 location(s) · Assistance Publique - Hôpitaux de Paris · NCT05917496A Clinical Trial of EHT102 Injection in Pediatric Patients With Biallelic hOTOF Mutations
Phase 1/Phase 2 · 1 location(s) · Shanghai Euhearing Therapeutics Co., Ltd · NCT07288580Monogenic Diabetes Misdiagnosed as Type 1
Phase N/A · 1 location(s) · McGill University Health Centre/Research Institute of the Mc · NCT03988764Cochlear Implants in Young Children With SSD
NA · 1 location(s) · University of North Carolina, Chapel Hill · NCT05775367National Registry of Rare Kidney Diseases
Phase N/A · 1 location(s) · UK Kidney Association · NCT06065852A Study to Investigate the Safety of OpCT-001 in Adults Who Have Primary Photoreceptor Disease (CLARICO)
Phase 1/Phase 2 · 5 location(s) · BlueRock Therapeutics · NCT06789445Long-Term Outcomes of Children With Congenital CMV in New York State
Phase N/A · 1 location(s) · Stony Brook University · NCT06226558Adaptive Optics Imaging of Outer Retinal Diseases
Phase N/A · 2 location(s) · Food and Drug Administration (FDA) · NCT05355415Wolfram Syndrome and WFS1-related Disorders International Registry and Clinical Study
Phase N/A · 1 location(s) · Washington University School of Medicine · NCT02841553GROWing Up With Rare GENEtic Syndromes
Phase N/A · 1 location(s) · dr. Laura C. G. de Graaff-Herder · NCT04463316Observational Study to Investigate the Short-term Effects of Transcorneal Electrical Stimulation on Visual Performance
Phase N/A · 1 location(s) · Okuvision GmbH · NCT07548944
Look up another condition
Patient organization or foundation? You can brand this page for your community — your logo, your resources, same honest registry data, kept current daily. Ask about branding →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.