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 ZonnenbergStuart B Hooper, Arjan Pas te

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

6 Downloads (Pure)

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

Fingerprint

Dive into the research topics of 'Physiological-based cord clamping in very preterm infants: the Aeration, Breathing, Clamping 3 (ABC3) trial-study protocol for a multicentre randomised controlled trial'. Together they form a unique fingerprint.

Cite this