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Clinical Trials/NCT07315594
NCT07315594
Not yet recruiting
Not Applicable

Cluster Randomized Trial of Initial Oxygen Concentration at Birth in Late-Preterm Infants

University of Alberta1 site in 1 country1,520 target enrollmentStarted: July 1, 2026Last updated:

Overview

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
1,520
Locations
1
Primary Endpoint
Need for ongoing respiratory support within the 1st hour after birth

Overview

Brief Summary

This study is aims to examine the best amount of oxygen to give preterm babies (born between 32 and 35 weeks) right after birth.

In the past, doctors used high levels of oxygen, but research has shown that using lower levels might help reduce the risk of death in full-term babies without harming brain development. However, investigators don't know the best oxygen level for babies born a little early (32 to 35 weeks). Some early data suggests that giving lower oxygen levels (FiO2 0.3) may not help babies reach healthy oxygen levels by 5 minutes after birth. This study will compare two oxygen levels-FiO2 0.6 and FiO2 0.3 to see which helps babies breathe better and need less ongoing breathing support. Researchers will study over 1,500 babies in hospitals across Alberta, Canada, to find the safest approach for these babies.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Treatment
Masking
None

Masking Description

Blinding will not be feasible, as each center will be assigned to each study intervention and then switch to the second intervention group. However, the trial statistician and DSMB will be blinded to group allocation.

Eligibility Criteria

Ages
0 Minutes to 10 Minutes (Child)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • i) Infants with gestational age between 32+0-35+6 weeks based on best available obstetrical estimate, requiring respiratory support
  • ii) Infants designated to receive full resuscitation, i.e., no parental request or pre-determined decision to provide only comfort care at birth
  • iii) No known major congenital or chromosomal malformation.

Exclusion Criteria

  • i) Infant born outside of study centers and transported to centers after delivery.

Arms & Interventions

Initial use of 60% oxygen during breathing support in the delivery room

Experimental

Infants randomized to the 60% Oxygen (FiO₂) Group will begin respiratory support with an initial inspired oxygen concentration of 60%. At birth, all infants will receive 60 seconds of delayed cord clamping as standard care. Following cord clamping, a pulse oximeter will be applied to measure peripheral oxygen saturation (SpO₂), with a reliable signal typically available at approximately 3 minutes of age.

At 3 minutes of age, the clinical team will assess SpO₂. If SpO₂ is <85%, the inspired oxygen concentration will be increased by 20% every 60 seconds to achieve an SpO₂ >85% by 5 minutes of age. If SpO₂ is >95% at or before 5 minutes of age, the inspired oxygen concentration will be decreased stepwise in increments of 10-20% every 60 seconds to maintain an SpO₂ >85% between 5 and 10 minutes of age, or an SpO₂ of 90-95% at and beyond 10 minutes of age.

Intervention: 60% Oxygen Group - Infants will start in 60% oxygen (Drug)

Initial use of 30% oxygen during breathing support in the delivery room

Active Comparator

Infants randomized to the 30% Oxygen (FiO₂) Group will begin respiratory support with an initial inspired oxygen concentration of 30%. At birth, all infants will receive 60 seconds of delayed cord clamping as standard care. Following cord clamping, a pulse oximeter will be applied to measure peripheral oxygen saturation (SpO₂), with a reliable signal typically available at approximately 3 minutes of age.

At 3 minutes of age, the clinical team will assess SpO₂. If SpO₂ is <85%, the inspired oxygen concentration will be increased by 20% every 60 seconds to achieve an SpO₂ >85% by 5 minutes of age. If SpO₂ is >95% at or before 5 minutes of age, the inspired oxygen concentration will be decreased stepwise in increments of 10-20% every 60 seconds to maintain an SpO₂ >85% between 5 and 10 minutes of age, or an SpO₂ of 90-95% at and beyond 10 minutes of age.

Intervention: 30% Oxygen Group - Infants will start in 30% oxygen (Drug)

Outcomes

Primary Outcomes

Need for ongoing respiratory support within the 1st hour after birth

Time Frame: first 60 minutes after birth

Ongoing respiratory support will be defined as: the need for intubation and mechanical ventilation or the use of any non-invasive respiratory supports (e.g., CPAP, nasal high flow therapy or low flow oxygen) after initial resuscitation

Secondary Outcomes

  • Mortality in the delivery room(first 60 minutes after birth)
  • Mortality prior discharge(up to 100 days after birth)
  • Duration of hospital stay(up to 100 days)
  • Air leak(first 72 hours after birth)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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