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Effects of Delayed Cord Clamping in Very Low Birth Weight Infants

Effects of Delayed Cord Clamping in Very Low Birth Weight (VLBW) Infants

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00840983
Enrollment
72
Registered
2009-02-11
Start date
2003-08-31
Completion date
2006-12-31
Last updated
2015-11-30

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

Conditions

Bronchopulmonary Dysplasia, Intraventricular Hemorrhage, Late Onset Neonatal Sepsis, Motor Skills Disorders, Necrotizing Enterocolitis

Keywords

delayed cord clamping, very low birthweight infant, bronchopulmonary dysplasia, intraventricular hemorrhage, motor function

Brief summary

The purpose of this study was to see if a brief delay in cord clamping for 30 to 45 seconds would result in higher hematocrit levels, fewer transfusions, healthier lungs, and better motor function at 40 wks and 7 months of age.

Detailed description

When cord clamping is delayed at birth or the cord is milked, infants receive a placental transfusion of 10-15 mL/kg during the first few minutes of life. This additional blood improves hemodynamic stability and may reduce the risk of intraventricular hemorrhage (IVH) and the vulnerability of infants to inflammatory processes. This blood also contains stem cells that are important in repairing tissue and building immunocompetence. The current randomized controlled trial prospectively tested the effects of DCC for 30-45 seconds followed by 1 cord milking with the aim of confirming our prior work and providing long-term follow-up. Our a priori hypotheses were that DCC would reduce the incidence of IVH, LOS, and result in better motor function at 18-22 months.

Interventions

PROCEDUREdelayed cord clamping

cord clamping was delayed for 30 to 45 seconds and infant was held lower than the level of the placenta

Sponsors

National Institute of Nursing Research (NINR)
CollaboratorNIH
Thrasher Research Fund
CollaboratorOTHER
University of Rhode Island
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
No

Inclusion criteria

* Women pregnant with gestation 24 to 31.6 weeks of singleton pregnancy by obstetrical evaluation * Obstetrician's approval of enrollment into study * Parental consent * Any mode of birth will be included

Exclusion criteria

* Obstetrician's refusal to enroll infants * Parental refusal for consent * Prenatally-diagnosed major congenital anomalies \[or multiple gestations\] * Intent to withhold or withdraw care * Severe or multiple maternal illnesses, frank vaginal bleeding, placenta abruption or previa * Mothers who are institutionalized or psychotic

Design outcomes

Primary

MeasureTime frame
VLBW infants in the delayed clamped group will have less chronic lung disease at 36 weeks postmenstrual age compared to VLBW infants in the immediate cord clamped grouped36 wks postmenstrual age
VLBW infants in the delayed clamped group will have fewer incidences of suspected necrotizing enterocolitis during the NICU stay when compared with VLBW infants in the immediate cord clamped groupHospital discharge
VLBW infants in the delayed clamped group will have better motor function by 6 to corrected age when compared with VLBW infants in the immediate cord clamped group7 months corrected age

Secondary

MeasureTime frame
Infants in the delayed cord clamping group will have less IVH than infants in the immediate clamping groupNICU stay
Infants in the delayed clamping group will hvae less late onset sepsis than infants in the immediate clamping group.NICU Stay

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026