30% or 60% Oxygen at Birth to Improve Neurodevelopmental Outcomes in Very Low Birthweight Infants

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age0-10
SponsorUniversity of Alberta

About this trial

Preterm birth, or birth before 37 weeks' gestation, is increasingly common, occurring in 8 percent of pregnancies in Canada. Preterm birth is associated with many health complications, particularly when the birth happens before 29 weeks' gestation. At this gestational age, the lungs are not fully developed and it is not uncommon for infants to have problems breathing at the time of birth. One complication that can arise is when an infant stops breathing and needs to be resuscitated. When preterm babies need to be resuscitated doctors must take special care because of the small infant size and the immaturity of the brain and lungs. Oxygen is used to resuscitate babies who need it, but unfortunately there is disagreement about the best oxygen concentration to use. Oxygen concentration is important because both too much and too little oxygen can cause brain injury. This research aims to fill this knowledge gap by participating in an international clinical trial to compare the effects of resuscitating babies less than 29 weeks' gestational age with either a low oxygen concentration or a high oxygen concentration. The oxygen concentrations have been selected using the best available knowledge.

This will be a cluster randomized trial where each participating hospital will be randomized to either 30 or 60 percent oxygen for the recruitment of 30 infants, and afterwards randomized to the other group for the recruitment of another 30 infants. After the trial, the investigator will determine whether the babies resuscitated with low oxygen or those resuscitated with high oxygen have better survival and long-term health outcomes. This research fills a critical knowledge gap in the care of extremely preterm babies and will impact their survival both here in Canada and internationally.

Eligibility criteria

Qualifiers

Infants born at 23 0/7 weeks to 28 6/7 weeks' gestational age who will receive full resuscitation and are without major congenital abnormalities

Disqualifiers

Infants who are outborn - initial resuscitation not performed at the study centre

Infants who are not born within the eligible gestational age range- this trial is specific to preterm infants

Infants who are born with a major congenital abnormality- congenital abnormalities may affect oxygenation or neurodevelopmental outcomes

Infants who will not receive full resuscitation at birth- these infants will not receive resuscitation

Trial design

Treatments tested in this trial

  • 30% oxygen group
  • 60% oxygen group

Treatment groups

1,200 Participants
are divided into 2 treatment groups

Sponsors and collaborators

University of Alberta

Lead sponsor

University of Toronto

Collaborator

University of Sydney

Collaborator

Dalhousie University

Collaborator

McMaster University

Collaborator

University of Manitoba

Collaborator

McGill University

Collaborator

University of Calgary

Collaborator

Memorial University of Newfoundland

Collaborator

University College Cork

Collaborator

University of British Columbia

Collaborator

Laval University

Collaborator

Université de Montréal

Collaborator

University of Ottawa

Collaborator

Queen's University

Collaborator

Université de Sherbrooke

Collaborator