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Physiological-based cord clamping in very preterm infants: the Aeration, Breathing, Clamping 3 (ABC3) trial-study protocol for a multicentre randomised controlled trial

  • Ronny Knol*
  • , Emma Brouwer
  • , Thomas Akker van den
  • , Philip DeKoninck
  • , Enrico Lopriore
  • , W. Onland
  • , Marijn Vermeulen
  • , Elske Akker van den
  • , Leti Bodegem van
  • , Willem P de Boode
  • , Anton H. van Kaam
  • , Irwin K M Reiss
  • , Graeme R Polglase
  • , Jeroen Hutten
  • , Sandra Prins
  • , Estelle Mulder
  • , Christiaan V Hulzebos
  • , Sam Janneke Samsbeek
  • , Mayke Putten van der
  • , Inge Zonnenberg
  • Stuart B Hooper, Arjan Pas te
*Corresponding author for this work

Research output: Contribution to journal › Article › Academic › peer-review

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Abstract

Background: International guidelines recommend delayed umbilical cord clamping (DCC) up to 1 min in preterm infants, unless the condition of the infant requires immediate resuscitation. However, clamping the cord prior to lung aeration may severely limit circulatory adaptation resulting in a reduction in cardiac output and hypoxia. Delaying cord clamping until lung aeration and ventilation have been established (physiological-based cord clamping, PBCC) allows for an adequately established pulmonary circulation and results in a more stable circulatory transition. The decline in cardiac output following time-based delayed cord clamping (TBCC) may thus be avoided. We hypothesise that PBCC, compared to TBCC, results in a more stable transition in very preterm infants, leading to improved clinical outcomes. The primary objective is to compare the effect of PBCC on intact survival with TBCC. Methods: The Aeriation, Breathing, Clamping 3 (ABC3) trial is a multicentre randomised controlled clinical trial. In the interventional PBCC group, the umbilical cord is clamped after the infant is stabilised, defined as reaching heart rate > 100 bpm and SpO 2 > 85% while using supplemental oxygen < 40%. In the control TBCC group, cord clamping is time based at 30–60 s. The primary outcome is survival without major cerebral and/or intestinal injury. Preterm infants born before 30 weeks of gestation are included after prenatal parental informed consent. The required sample size is 660 infants. Discussion: The findings of this trial will provide evidence for future clinical guidelines on optimal cord clamping management in very preterm infants at birth. Trial registration: ClinicalTrials.gov NCT03808051. First registered on January 17, 2019.

Original languageEnglish
Article number838
Number of pages13
JournalTrials [E]
Volume23
Issue number1
DOIs
Publication statusPublished - 1 Oct 2022

Keywords

  • Cord clamping
  • Physiological-based cord clamping
  • Preterm infants
  • Randomised clinical trial
  • Study protocol
  • Cord clamping

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