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

Author:

Knol RonnyORCID,Brouwer Emma,van den Akker Thomas,DeKoninck Philip L. J.,Lopriore Enrico,Onland Wes,Vermeulen Marijn J.,van den Akker–van Marle M. Elske,van Bodegom–Vos Leti,de Boode Willem P.,van Kaam Anton H.,Reiss Irwin K. M.,Polglase Graeme R.,Hutten G. Jeroen,Prins Sandra A.,Mulder Estelle E. M.,Hulzebos Christian V.,van Sambeeck Sam J.,van der Putten Mayke E.,Zonnenberg Inge A.,Hooper Stuart B.,te Pas Arjan B.

Abstract

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 SpO2 > 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.

Funder

ZonMw

Gisela Thier Fund

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Medicine (miscellaneous)

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