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A Randomized Controlled Trial of Immediate versus Delayed Umbilical Cord Clamping in Preterm Infants of Multiple Births

A Randomized Controlled Trial of Immediate versus Delayed Umbilical Cord Clamping in Preterm Infants of Multiple Births

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20170125001
Enrollment
100
Registered
2017-01-25
Start date
2016-03-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

multiple births preterm infants delayed umbilical cord clamping delayed umbilical cord clamping preterm infants multiple births caesarian section

Interventions

In the DCC group&#44
after each infant is delivered and placed on the mother’s perineum (in case of vaginal delivery) or on the thigh (in case of caesarian section)&#44
the clamping and cutting of umbilical cord will be delayed for at least 30 seconds but not more than 60 seconds. During the first 30 second&#44
airway clearance&#44
drying&#44
suctioning&#44
and stimulating. In infants who response well to initial resuscitation&#44
the clamping and cutting of the cord will be delayed until 60 seconds. However&#44
in infants who do not responded to initial resuscitation or appear non&#45
the cord will be clamped and cut at 30 seconds or at any time during 30 to 60 seconds.,In the ICC group&#44
after each infant is delivered&#44
the umbilical cord will be clamped and cut immediately by obstetrician (less than 10 seconds).
Experimental Procedure/Surgery,Experimental Procedure/Surgery
Delayed cord clamping (DCC),Immediate cord clamping (ICC)

Sponsors

Faculty of Medicine Ramathibodi Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Pregnant women with multiple gestations who deliver preterm infants at gestational age (GA) of 28-36 weeks’ gestation (best estimation by their earliest ultrasound or last menstrual period) is eligible to participate in the study.

Exclusion criteria

Exclusion criteria: prenatally diagnosed major congenital anomaly in any infants, twin-to-twin transfusion syndrome (TTTS) or twin anemic-polycythemic sequence (TAPS), discordant twins (weight difference of more than 20%), any intrauterine fetal death, hydrops, antepartum or intrapartum hemorrhage such as placental abruption or uterine rupture, or declination by the medical team (obstetrician or pediatrician) in performing the intervention.

Design outcomes

Primary

MeasureTime frame
Infants' hematocrit level at birth On admission after birth Central Hematocrit (%)

Secondary

MeasureTime frame
Superior Vena Cava (SVC) Flow Within 24 hours after birth Echo-cardiogram measurement,Infants' hematocrit level after birth At 8 weeks after birth Central Hematocrit (%),Other Maternal and infants' relevance clinical outcomes During hospital admission Patients' chart review

Countries

Thailand

Contacts

Public ContactChayatat Ruangkit

Ramathibodi Hospital, Mahidol University

chayatatr@hotmail.com095-165-6605

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026