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Clinical study on the use of cut umbilical cord milking for neonates with placenta previa: a single-center randomized controlled clinical trial

Clinical study on the use of cut umbilical cord milking for neonates with placenta previa: a single-center randomized controlled clinical trial protocol

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500103506
Enrollment
Unknown
Registered
2025-05-30
Start date
2023-12-08
Completion date
Unknown
Last updated
2025-06-02

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

Conditions

Placenta previa

Interventions

study group:cut umbilical cord milking
control group:immediate cord clamping

Sponsors

Nanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medical School
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Newborn delivered through the penetrated placenta during previous cesarean section with placenta previa; (2) Singleton; (3) Gestational age >= 34 weeks.

Exclusion criteria

Exclusion criteria: (1) Newborns have chromosomal abnormalities or severe structural malformations; (2) Stillbirth.

Design outcomes

Primary

MeasureTime frame
Hemoglobin;—

Secondary

MeasureTime frame
Incidence of respiratory disease;Overall complication rate;Blood pressure;Heart rate;Meconium urine passage time;Hct;—

Countries

China

Contacts

Public ContactDai Yimin,Yang Ling

Nanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medical School

candyrain963@163.com+86 158 9584 0021

Outcome results

None listed

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