Crick
HomeTrialsGenesDrugs23andMeGraphBlogContact
  • Home
  • Trials
  • Genes
  • Drugs
  • 23andMe
  • Graph
  • Blog
  • Contact
Crick

An open-source clinical intelligence platform. Explore clinical trials, gene networks, and molecular structures using public data sources.

Data Sources

  • ClinicalTrials.gov
  • OpenTargets
  • ClinVar
  • PubChem

Links

  • Contact
  • About
  • Privacy

© 2026 Crick. All rights reserved.

Crick is for educational purposes only. Not medical advice.

Results for “Profound Congenital Deafness”

6 trials

Filters

Phase
Early Phase 1
Phase 1
Phase 2
Phase 3
Phase 4
Status
Recruiting
Active, Not Recruiting
Not Yet Recruiting
Completed
Enrolling by Invitation

Showing 6 of 6 results

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)Looking for participantsNCT06370351
What this trial is testing

A Phase I/II Clinical Trial with SENS-501 in Children Suffering from Severe to Profound Hearing Loss Due to Otoferlin (OTOF) Mutations

Who this might be right for
OTOF Gene MutationDFNB9Congenital Deafness+5 more
Sensorion 12
Not applicableLooking for participantsNCT05917496
What this trial is testing

Analysis of Parental Support in Families Using the LENA After Early Cochlear Implantation

Who this might be right for
Profound Congenital DeafnessCochlear Implantation
Assistance Publique - Hôpitaux de Paris 30
Not applicableNo Longer AvailableNCT02589912
What this trial is testing

Compassionate Use Arm - ABI541 ABI for 10 NF2 Patients

Who this might be right for
Neurofibromatosis Type 2Severe Profound Sensorineural Hearing Loss
Massachusetts Eye and Ear Infirmary
Not applicableLooking for participantsNCT05402813
What this trial is testing

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

Who this might be right for
Sensorineural Hearing Loss, BilateralAUNB1DFNB1A+4 more
Sensorion 180
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