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Exploring clinical research efficacy of delayed cord clamping on twins by vaginal delivery

Exploring clinical research efficacy of delayed cord clamping on twins by vaginal delivery

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100052956
Enrollment
Unknown
Registered
2021-11-06
Start date
2021-11-06
Completion date
Unknown
Last updated
2022-08-30

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

Conditions

Delayed cord clamping on twins by vaginal delivery

Interventions

intervention group:Delayed cord clamping lasted for at least 60 s after delivery
control group:Delayed cord clamping lasted for less than 30 s after delivery

Sponsors

Nantong University
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Double velvet double sheep twins; 2. Vaginal birth.

Exclusion criteria

Exclusion criteria: 1. Cancer; 2. The mother's blood system disease or moderate to severe anemia, blood quality level <99; 3. Severe liver and kidney disease; 4. Severe preeclampsia; 5. Diseases affecting fetal blood and bilirubin metabolism: placental abruption, placenta previa, rupture of blood vessels previa, etc.; 6. Twin-twin transfusion syndrome; 7. Postpartum deformity found (excluding mild deformity in appearance); 8. Shunt dissection; 9. Contraindications for vaginal delivery; intrauterine stillbirth; acute intrauterine distress; first-born death.

Design outcomes

Primary

MeasureTime frame
neonatal haemoglobin;Umbilical artery pH;—

Countries

China

Contacts

Public ContactZhang Feng

(School of Nursing) Medical College, Nantong University

zhangfeng820909@163.com+86 13814715979

Outcome results

None listed

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