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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
A Phase I/II Clinical Trial With SENS-501 in Children Suffering From Severe to Profound Hearing Loss Due to Otoferlin (OTOF) MutationsDeafness, Deafness, Autosomal Recessive 9, Ear Diseases, Hearing Loss, Sensorineural, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Sensation Disorders, Signs and Symptoms, hearing disorder, hearing loss disorder, nervous system disorder, otorhinolaryngologic diseaseActive, not recruitingPhase 1 / Phase 22026-07-08NCT06370351
Natural History in Children up to 16 Years With Mild to Profound Hearing Loss Due to Mutations in GJB2 / OTOF GenesEar Diseases, Hearing Loss, Sensorineural, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Sensation Disorders, Signs and Symptoms, autosomal recessive nonsyndromic hearing loss 1A, hearing disorder, hearing loss disorder, nervous system disorder, otorhinolaryngologic diseaseRecruitingNot stated2026-06-01NCT05402813
Cross-sectional and Prospective Study to Characterize Early-onset PresbycusisDeafness, Ear Diseases, Hearing Loss, Sensorineural, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Sensation Disorders, Signs and Symptoms, hearing disorder, hearing loss disorder, nervous system disorder, otorhinolaryngologic disease, presbycusisRecruitingNot stated2026-05-08NCT06354010