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A prospective study on the impact of couples factors on the prognosis of live birth and other factors in couples with recurrent pregnancy loss

A prospective study on the impact of couples factors on the prognosis of live birth and other factors in couples with recurrent pregnancy loss

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400080465
Enrollment
Unknown
Registered
2024-01-30
Start date
2024-02-01
Completion date
Unknown
Last updated
2024-02-05

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

Conditions

pregnancy loss

Interventions

Case group:N/A
Control group:N/A

Sponsors

The second hospital of Lanzhou University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: (1) A history of unintended pregnancy loss that meets the diagnosis of at least one pregnancy loss; (2) The age of the patient's spouse is between 18 and 45 years old; (3) Patient couples who agree to use their personal medical records for research purposes and sign informed consent.

Exclusion criteria

Exclusion criteria: (1) Have a history of taking anticoagulants, immunomodulators, and steroid drugs within the past 3 months; (2) If the couple's medical records are incomplete or there are significant missing data of interest.

Design outcomes

Primary

MeasureTime frame
24 weeks live birth rate;—

Secondary

MeasureTime frame
early pregnancy loss rate;clinically confirmed pregnancy rate;ongoing pregnancy rate(to 10 weeks);28 weeks live birth rate;ectopic pregnancy rate;stillbirth rate;incidence rate of pregnancy complications;neonatal weigh;neonatal Apgar score;neonatal birth defect rate;—

Countries

China

Contacts

Public ContactFang Wang

The second hospital of Lanzhou University

ery_fwang@lzu.edu.cn+86 139 1930 2888

Outcome results

None listed

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