Skip to content

Delayed Clamping and Milking the Umbilical Cord in Preterm Infants

Delayed Clamping and Milking the Umbilical Cord Prior to Clamping in Preterm Infants and the Effect of Neonatal Outcomes

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02092103
Enrollment
282
Registered
2014-03-19
Start date
2014-03-31
Completion date
2018-07-08
Last updated
2018-12-28

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

Conditions

Premature Birth

Keywords

Premature Birth, Umbilical Cord Clamping

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.

Interventions

PROCEDURECord Milking

See description in cord milking arm.

Sponsors

TriHealth Inc.
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Hemoglobin and Hematocrit values (H/H) in NICUNICU admission to discharge, expected average of 50 daysAll H/H values in the neonatal intensive care unit (NICU) will be recorded.

Secondary

MeasureTime frameDescription
Neonatal transfusionsBirth to discharge, expected average of 50 daysThe incidence of transfusions between the two groups will be compared.
Necrotizing enterocolitisBirth to discharge, expected average of 50 daysThe incidence of necrotizing enterocolitis between the two groups will be compared.
Intraventricular hemorrhageBirth to discharge, expected average of 50 daysThe incidence of intraventricular hemorrhage between the two groups will be compared.

Other

MeasureTime frameDescription
Length of stayBirth to discharge, expected average of 50 daysThe length of NICU stay between the two arms will be compared.
Survival to dischargeBirth to discharge, expected average of 50 daysThe rate of infant survival until discharge will be recorded for both groups.

Countries

United States

Outcome results

None listed

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