Skip to content

A prospective study of comprehensive carrier screening in reproductive centers

A prospective study of comprehensive carrier screening in reproductive centers

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600125654
Enrollment
Unknown
Registered
2026-05-29
Start date
2026-06-01
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Preconception genetic screening for couples planning to have children

Interventions

Observational group:None

Sponsors

Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Couples planning pregnancy or with a gestational age of 28 weeks or less; 2. Voluntarily participate in this study and sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Couples intending to use donated gametes for reproduction; 2. Those who have received blood transfusions, organ transplants, or immunotherapy within the past year; 3. Spouses unable to cooperate with testing; 4. Vulnerable groups other than pregnant women, including people with mental illness, cognitive impairment, critically ill patients, minors, and the illiterate.

Design outcomes

Primary

MeasureTime frame
Carrier rate in couples;Detection rate in high-risk couples;Variant carrier rate;Gene carrier rate;Reproductive outcomes;

Countries

China

Contacts

Public ContactJin Jiamin

Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University

11718252@zju.edu.cn+86 571 88778969

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026