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Study of hearing loss

Congenital Hearing Loss: Genetic factors underlying Non-syndromic Hearing loss

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2017/04/008414
Enrollment
700
Registered
2017-04-26
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- Non-syndromic hearing loss

Interventions

None listed

Sponsors

Dr Saadi Abdul Vahab
Lead Sponsor
Dr K Satyamoorthy
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1. Hearing loss greater than 25Db 2. Sensorineural type of loss 3. Hearing loss persistent and congenital 4. Hearing loss can be progressive or non progressive 5. Hearing loss present in both the ears

Exclusion criteria

Exclusion criteria: Syndromic conditions 1. Conductive hearing loss 2. Acquired hearing loss

Design outcomes

Primary

MeasureTime frame
Mutations causing SNHL may be identified at the end of the study.Timepoint: By March 2020—

Secondary

MeasureTime frame
NILTimepoint: NIL—

Countries

India

Contacts

Public ContactDr Jayashree S Bhat

KMC Hospital, Attavar

bhat.js@manipal.edu9900514692

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026