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Clinical multi-center study on preimplantation diagnosis of hereditary deafness in China

Clinical multi-center study on preimplantation diagnosis of hereditary deafness in China

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000033014
Enrollment
Unknown
Registered
2020-05-18
Start date
2020-09-01
Completion date
Unknown
Last updated
2020-05-18

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

Conditions

hereditary hearing loss

Interventions

Hereditary hearing loss PGD family:Genetic diagnosis of hearing loss

Sponsors

Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Families at high risk of hereditary hearing loss received and taught by the participating units. All participants are required to sign an informed consen.

Exclusion criteria

Exclusion criteria: (1) Families who explicitly refuse to participate in the project after accepting missions; (2) Diagnosed with deafness caused by non-genetic factors.

Design outcomes

Primary

MeasureTime frame
Deafness genes;—

Countries

China

Contacts

Public ContactDai Pu

Chinese PLA General Hospital

daipu301@vip.sina.com+86 13910213511

Outcome results

None listed

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