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Establishment of methodology for carrier screening of single-gene genetic diseases in Chinese population

Establishment of methodology for carrier screening of single-gene genetic diseases in Chinese population

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100050723
Enrollment
Unknown
Registered
2021-09-03
Start date
2021-09-15
Completion date
Unknown
Last updated
2022-05-02

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

Conditions

monogenic disorders

Interventions

Infertility group:Prenatal diagnosis

Sponsors

Obstetrics and Gynecology Hospital affiliated to Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Both husband and wife are in good health and have no serious genetic diseases; 2. The direct family members within three generations of both husband and wife have no family history of hereditary diseases; 3. The age of both spouses is less than 45 years old; 4. Both spouses have no history of malignant tumor and radiation exposure.

Exclusion criteria

Exclusion criteria: 1. One of the spouses is a non-Chinese patient; 2. Consanguineous couples.

Design outcomes

Primary

MeasureTime frame
pathogenic variant;—

Countries

China

Contacts

Public ContactXu Chenming

Obstetrics and Gynecology Hospital affiliated to Fudan University

chenming_xu2006@163.com+86 21 64073897

Outcome results

None listed

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