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NCT07024524

Perceptual Evaluation and Rehabilitation System Development for Congenital Hearing Loss

Recruiting now NA Last updated 28 July 2025
What this trial tests

NA trial testing Rehabilitation training in Congenital Hearing Loss in 210 participants. Currently enrolling.

Timeline
4 July 2025
Primary endpoint
1 January 2028
5 May 2028

Quick facts

Lead sponsorEye & ENT Hospital of Fudan University
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposeother
Enrollment210
Start date4 July 2025
Primary completion1 January 2028
Estimated completion5 May 2028
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Eye & ENT Hospital of Fudan University

Who can join

Adults 1 to 35, any sex, with Congenital Hearing Loss or Gene Therapy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study aims to establish a novel multimodal evaluation and precision rehabilitation system for patients with congenital hearing loss who have received hearing aids, cochlear implantation, or emerging gene therapy. The proposed system will integrate age-stratified difficulty levels, combined with a gamified interaction platform or software designed to assess and train three core perceptual domains: auditory speech perception, music perception, and spatial hearing capabilities.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Rehabilitation training

Trials testing the same drug.

Other recruiting trials for Congenital Hearing Loss

Currently open trials in the same condition.

Other Eye & ENT Hospital of Fudan University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07024524.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing