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Results for “Congenital Deafness”

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Showing 20 of 0 results

Testing effectiveness (Phase 2)Looking for participantsNCT05788536
What this trial is testing

DB-OTO, an Adeno-Associated Virus (AAV) Based Gene Therapy, in Children/Infants, Adolescents and Adults With Hearing Loss Due to Otoferlin Mutations

Who this might be right for
Congenital Hearing Loss Secondary to Biallelic Mutations of the Otoferlin Gene (OTOF)
Regeneron Pharmaceuticals 36
Testing effectiveness (Phase 2)Study completedNCT02497690
What this trial is testing

Effectiveness of Therapy Via Telemedicine Following Cochlear Implants

Who this might be right for
Congenital Sensorineural Deafness
University of Colorado, Denver 77
Not applicableStudy completedNCT04622059
What this trial is testing

AUditive Direct In-utero Observation (AUDIO): Prenatal Testing of Congenital Hypoacusis

Who this might be right for
Hearing Loss
Elena Contro 210
Not applicableStudy completedNCT03875339
What this trial is testing

Communities Helping the Hearing of Infants by Reaching Parents

Who this might be right for
Congenital Hearing Loss
Matthew Bush, MD 2,699
Early research (Phase 1)Study completedNCT02102256
What this trial is testing

A Safety Study of the Auditory Brainstem Implant for Pediatric Profoundly Deaf Patients

Who this might be right for
Profound Bilateral Deafness Due toBilateral Cochlear AplasiaBilateral Cochlear Nerve Deficiency+1 more
Laurie Eisenberg 10
Not applicableEnded earlyNCT00004345
What this trial is testing

Study of Dietary N-3 Fatty Acids in Patients With Retinitis Pigmentosa and Usher Syndrome

Who this might be right for
Usher SyndromeRetinitis Pigmentosa
National Center for Research Resources (NCRR) 100
Not applicableWithdrawnNCT06019481
What this trial is testing

A Natural History Study in Pediatric Participants With Hearing Loss Due to OTOF, GJB2, or GJB2/GJB6 Mutations

Who this might be right for
Congenital Hearing Loss Secondary to Biallelic Mutations in the Otoferlin Gene (OTOF)Biallelic Mutations in the Gap Junction Beta 2 (GJB2) GeneDigenic Mutations in GJB2/Gap Junction Beta 6 (GJB6) Genes
Regeneron Pharmaceuticals
Not applicableNot Yet RecruitingNCT07786545
What this trial is testing

Pilot Evaluation of the Developed Syntactic-Semantic Visual Configuration Intervention for Children With Language Impairment

Who this might be right for
Language ImpairmentAutismHearing Impaired Children+1 more
Riphah International University 20
Not applicableUnknownNCT05764980
What this trial is testing

Neurovisual Function in CHARGE Syndrome

Who this might be right for
CHARGE Syndrome
Fondazione Policlinico Universitario Agostino Gemelli IRCCS 20
Not applicableStudy completedNCT03901391
What this trial is testing

Prospective Open Clinical and Genetic Study of Patients With Retinitis Pigmentosa

Who this might be right for
Retinitis PigmentosaUsher Syndromes
Sensor Technology for Deafblind 130
Not applicableNot Yet RecruitingNCT07358728
What this trial is testing

OSIA System Bilateral Implantation Efficacy Evaluation in Children With Ear Aplasia

Who this might be right for
Deafness Caused by High Grade Microtia or Ear Atresia
Assistance Publique - Hôpitaux de Paris 12
Testing effectiveness (Phase 2)Study completedNCT04604548
What this trial is testing

The KHENEREXT Study

Who this might be right for
Mitochondrial DiseasesMitochondrial DNA tRNALeu(UUR) m.3243A<G MutationMaternally Inherited Diabetes and Deafness (MIDD)+2 more
Khondrion BV 11
Not applicableStudy completedNCT04202185
What this trial is testing

Evaluation of a Cohort of Congenital Deep Deafness Patients and/or With Auditory Neuropathy, Looking for DFNB9

Who this might be right for
Congenital Profound Hearing Loss
Assistance Publique - Hôpitaux de Paris 150
Testing effectiveness (Phase 2)Study completedNCT05972954
What this trial is testing

OMT-28 in Patients With Primary Mitochondrial Disease (PMD) (PMD-OPTION)

Who this might be right for
Primary Mitochondrial Disease
Omeicos Therapeutics GmbH 28
Large-scale testing (Phase 3)Not Yet RecruitingNCT07710196
What this trial is testing

A 24-Month Trial of NPI-001 for the Preservation of Photoreceptors in Retinitis Pigmentosa Associated With Usher Syndrome

Who this might be right for
Retinitis Pigmentosa (RP)Usher Syndrome
Nacuity Pharmaceuticals, Inc. 80
Not applicableStudy completedNCT00231010
What this trial is testing

Molecular Genetics of Retinal Degenerations

Who this might be right for
Retinal DegenerationRetinitis Pigmentosa
National Eye Institute (NEI) 3,549
Not applicableStudy completedNCT00341874
What this trial is testing

Genetic Analyses of Nonsyndromic and Syndromic Deafness in Pakistan

Who this might be right for
Hearing Disorder
National Institute on Deafness and Other Communication Disorders (NIDCD) 18,009
Early research (Phase 1)Not Yet RecruitingNCT06592131
What this trial is testing

BF844 Safety and Pharmacokinetic Study in Healthy Volunteers

Who this might be right for
Usher Syndrome Type 3
EyeXCel Pty. Ltd. 76
Testing effectiveness (Phase 2)Looking for participantsNCT06591793
What this trial is testing

Study of Subretinally Injected AAVB-081 in Patients With Usher Syndrome Type IB (USH1B) Retinitis Pigmentosa

Who this might be right for
Usher Syndrome, Type 1B
AAVantgarde Bio Srl 15
Large-scale testing (Phase 3)Study completedNCT02005822
What this trial is testing

Congenital Cytomegalovirus: Efficacy of Antiviral Treatment

Who this might be right for
Congenital Cytomegalovirus InfectionSensorineural Hearing Loss
Dr. Ann C.T.M. Vossen 37
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