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Delayed Clamping and Milking the Umbilical Cord in Preterm Infants

Not Applicable
Completed
Conditions
Premature Birth
Interventions
Procedure: Cord Milking
Registration Number
NCT02092103
Lead Sponsor
TriHealth Inc.
Brief Summary

This is a randomized controlled trial that will compare the effects of delayed umbilical cord clamping to umbilical cord milking in preterm infants (less than 34 weeks gestation). The infants' hemoglobin and hematocrit levels in the Neonatal Intensive Care Unit (NICU) will be evaluated, as well as the rates of necrotizing enterocolitis, intraventricular hemorrhage, and blood transfusions. The hypothesis is that milking the umbilical cord prior to clamping is superior to simply delayed cord clamping, presumably providing an increased blood volume to the preterm neonate improving its outcomes.

Detailed Description

The optimal timing for clamping the umbilical cord after birth in preterm infants has been a subject of controversy and debate for many years. It has been until recently the standard practice in ob/gyn to clamp the umbilical cord immediately post delivery to allow for immediate transition resuscitation of the neonate, especially in preterm infants. Due to the fact that optimal timing for cord clamping has yet to be definitively established in the preterm population, more information is needed. Immediate cord clamping, however, could preclude the infant from an extra boost in blood volume that may prove beneficial later in the newborn life. Directly comparing the recently recommended practice of delayed umbilical cord clamping to milking the umbilical cord prior to clamping has the potential to prove beneficial for the neonates in question, as well as change daily obstetrical practices. In this study all infants below 34 weeks will be randomized into one of two groups: delayed cord clamping and milking the umbilical cord prior to clamping. The decision was made not to include immediate cord clamping due to a recent American Congress of Obstetricians and Gynecologists (ACOG) recommendation that all preterm infants have their cord clamping be delayed. Their outcomes will be measured by serial hemoglobin and hematocrit levels while in the NICU, the incidence of necrotizing enterocolitis, incidence of intraventricular hemorrhage, and the need for neonatal blood transfusions.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
282
Inclusion Criteria
  • Admitted to Labor & Delivery at Good Samaritan TriHealth Hospital in Cincinnati, Ohio with expected/possible preterm delivery between 23-34 weeks gestation
  • Care provided by Good Samaritan TriHealth Hospital's Faculty Medical Center or Tri-State Maternal Fetal Medicine
Exclusion Criteria
  • Declined to participate
  • Known congenital anomalies
  • Precipitous delivery preventing completion of the protocol
  • Placental abruption around the time of or as indication for delivery
  • Mother has uterine rupture
  • Non reassuring fetal heart tracing (FHT) immediately prior/leading to delivery
  • Multiple gestation
  • Parvo B19
  • Infants known to be at risk of anemia due to isoimmunization (mother has red blood cell antibodies

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Cord MilkingCord MilkingInfants randomized to the cord milking group will follow the protocol below: 1. Infant held at or below level of perineum (vaginal delivery) or incision (cesarean delivery) 2. Infant held and the cord is milked from perineum to infant four times 3. Assistant to deliver preps cord clamps 4. Cord clamped and cut 5. Infant handed off to waiting staff
Primary Outcome Measures
NameTimeMethod
Hemoglobin and Hematocrit values (H/H) in NICUNICU admission to discharge, expected average of 50 days

All H/H values in the neonatal intensive care unit (NICU) will be recorded.

Secondary Outcome Measures
NameTimeMethod
Necrotizing enterocolitisBirth to discharge, expected average of 50 days

The incidence of necrotizing enterocolitis between the two groups will be compared.

Intraventricular hemorrhageBirth to discharge, expected average of 50 days

The incidence of intraventricular hemorrhage between the two groups will be compared.

Neonatal transfusionsBirth to discharge, expected average of 50 days

The incidence of transfusions between the two groups will be compared.

Trial Locations

Locations (1)

Good Samaritan TriHealth Hospital

🇺🇸

Cincinnati, Ohio, United States

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