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NCT Number: NCT03657394

Comparative Outcomes Related to Delivery-room Cord Milking In Low-resourced Kountries

The investigators will conduct a study on non-vigorous infants at birth to determine if umbilical cord milking (UCM) results in lower rate of moderate to severe hypoxic ischemic encephalopathy (HIE) or death than early clamping and for infants who are non-vigorous at birth and need immediate resuscitation.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Age range

35 week–42 week

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

KLE Academy of Higher Education and Research (Deemed-to-be-University) Jawaharlal Nehru Medical College, Belagavi, Karnataka, India

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About this study

Hypoxic-ischemic encephalopathy (HIE) is a brain injury caused by inadequate blood flow and oxygen delivery to the neonatal brain. Almost all infants with severe HIE and 30-50% infants with moderate HIE either die or develop significant developmental delay, cerebral palsy or other disabilities.The incidence of HIE is 1-3 per 1,000 term births in developed countries and 15-20 times higher in developing countries (Worldwide, 0.5 to 1 million infants develop HIE each year). Therapeutic hypothermia is the only proven therapy for infants with HIE. Even after receiving therapeutic hypothermia, one-half of all infants with moderate and severe HIE die or develop neurological and functional impairment. Therapeutic hypothermia is not widely available and ineffective in developing nations.There is an urgent need for a new therapy for neonates with HIE, which can complement hypothermia and be readily available in developing nations. Stem cell transplantation is a potential therapy for infants with HIE. Umbilical cord blood is a rich source of stem cells. Umbilical cord milking (UCM) may have similar effect as autologous umbilical cord blood cell transplantation.

Preliminary evidence suggests a placental transfusion in term infants may be a neuroprotective mechanism that can also facilitate cardiovascular transition for neonates depressed at birth and result in decreased mortality and improved neurodevelopmental outcomes. Infants with HIE, due to varied complications during the birth process, have poor perfusion due to fetal blood volume loss to the placenta. However, the most common method of providing placental blood, delayed cord clamping (DCC) cannot be performed since infants with HIE are non-vigorous and providers often need to perform resuscitation immediately after birth. The World Health Organization and the American College of Obstetrics and Gynecology (ACOG) also does not recommended DCC in neonates who are non-vigorous (limp, pale, and not breathing) at birth and require immediate resuscitation. Umbilical cord milking (UCM) or gently squeezing cord blood toward the baby, is an alternative to DCC, which can achieve significant placental transfusion without delaying resuscitation. Further, UCM can be completed as quickly as immediate cord clamping (ICC) and UCM requires minimal training and no additional staff.

The investigators hypothesized that UCM will reduce the number of infants developing moderate to severe HIE or death in neonates who are non-vigorous at birth compared to early cord clamping (ECC). This will be a cluster crossover randomized controlled trial. Each hospital will be randomly assigned to use either ECC or UCM for any infant who is non-vigorous at birth and needing resuscitation over a period of 6 months. Then the site will change to the other method for an additional 6 months.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Non-vigorous neonates born between 35-42 weeks

Exclusion criteria

  • Congenital malformation of CNS.
  • Chromosomal abnormalities.
  • Major congenital malformations.
  • Abruption/cutting through the placenta at delivery.
  • Umbilical cord knots or inadequate cord length.
  • Mono-chorionic twins or twins with no information on amnion/chorion.
  • Multiple gestation >2 .

Treatment and study plan

Umbilical Cord Milking

Other

At delivery, the umbilical cord is grasped, and blood is pushed toward the infant 4 times before the cord is clamped. This procedure infuses a placental transfusion of blood into the infant and can be done in 1--15 seconds.

Primary outcomes

  1. Moderate to severe HIE or death

    Time frame: From date of birth until the date of discharge from the hospital or date of death from any cause, whichever come first, asessed up to 10 weeks.

    Number of infants with moderate to severe HIE or death

Secondary outcomes

  1. MRI of the brain

    Time frame: 4 days to 2 weeks

    Number of infants with moderate to severe HIE who have abnormal brain MRI

Sponsors and collaborators

Lead sponsor

Nemours Children's Clinic

Other

Collaborators

  • All India Institute of Medical Sciences
  • Daga Memorial Maternity and Children's Hospital, Nagpur, India
  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
  • Government Medical College, Nagpur
  • Indira Gandhi Government Medical College & Hospital, Nagpur, India
  • Jawaharlal Institute of Postgraduate Medical Education & Research
  • Jawaharlal Nehru Medical College
  • Karnataka Institue of Medical Sciences, Hubbali, India
  • Mahatma Gandhi Institute of Medical Sciences
  • Pimpri Chinchwad Municipal Corporation's Post-Graduate Institute, Yashwantrao Chavan Memorial Hospital, Pune, India
  • Sharp HealthCare
  • St. Louis University
  • Thomas Jefferson University
  • University of San Diego

Registry information

Official study title

A Cluster Randomized Clinical Trial of Umbilical Cord Milking Versus Early Cord Clamping on Short and Long-term Outcomes in Neonates Who Are Non-Vigorous at Birth

Acronym: CORDMILK

Important dates

Study start
2022
Primary completion
2025
Study completion
2026
First posted
Sep 5, 2018
Registry last updated
Feb 13, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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