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Investigation and clinical intervention study on genetic screening of deaf children

Investigation and clinical intervention study on genetic screening of deaf children

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-EOC-16009641
Enrollment
Unknown
Registered
2016-10-26
Start date
2016-12-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Hereditary hearing impairment

Interventions

Target population:Knowledge of disease prevention measures and hereditary deafness Knowledge

Sponsors

Xinhua hospital affiliated to Shanghai Jiao Tong University School of medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 10 Years

Inclusion criteria

Inclusion criteria: 1. living in Shanghai for more than 5 years; 2. The hearing loss children (standard air conduction threshold is greater than 40dB); 3. The hearing loss occured before 10 years old.

Exclusion criteria

Exclusion criteria: 1. The conductive deafness or mixed deafness; 2. The noise induced deafness; 3. Who decide to leave for any reason.

Design outcomes

Primary

MeasureTime frame
genetic deafness of birth defects;—

Countries

China

Contacts

Public ContactYan Ma

Shanghai Xinhua Hospital

mayanent@126.com+86 13661850296

Outcome results

None listed

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