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Clinical Trials in Denmark / NCT06849596
Recruiting Not applicable

Manual T-piece Versus Ventilator Positive Pressure Ventilation During Resuscitation of Extremely Premature Neonates

NCT06849596 · tracked via the Priya Life Science Denmark tracker
Sponsor
Michelle Baczynski
Phase
Not applicable
Started
2025-12-01
Last updated
2026-06-11

Condition(s) studied

Neonatal ResuscitationApnea Neonatal

Investigational drug(s) / intervention(s)

Ventilator derived positive pressure ventilation - V-PPVT-piece resuscitator (TPR)

Ventilator derived positive pressure ventilation - V-PPV: The clinical team will determine the need for PPV, as per local practice and Neonatal Resuscitation Program. Each site will be previously randomized to their method of providing PPV for preterm neonates during the first 10 minutes after birth. Ventilator delivered positive pressure ventilation (V-PPV) using a nasal interface will be delivered to the infant in the resuscitation room.

T-piece resuscitator (TPR): The clinical team will determine the need for PPV, as per local practice and Neonatal Resuscitation Program. Each site will be previously randomized to their method of providing PPV for preterm neonates during the first 10 minutes after birth. PPV will be provided with a T-piece resuscitator (Neopuff, Fisher \& Paykel Healthcare) connected to an appropriately sized face-mask.

Study summary

Many extremely premature infants require immediate help with breathing after birth. Positive pressure ventilation (PPV) using a device called a T-piece resuscitator is a common method. PPV is needed to establish proper lung function, improve gas exchange, and encourage the infant to breathe spontaneously. However, T-piece resuscitators have limitations, like a lack of visual feedback and variable settings, which may result in reduced effectiveness of PPV. Improving PPV effectiveness may reduce the need for more invasive procedures, such as intubation, which pose an increased risk of complications and death for these fragile infants. A novel approach, that may overcome the above limitations and deliver PPV with precise settings through a nasal mask, is to use a ventilator to deliver PPV (V-PPV) using a respiratory mode called nasal intermittent positive pressure ventilation (NIPPV). While NIPPV is commonly used in neonatal intensive care units to support breathing in premature infants, the impact of V-PPV use during immediate post-birth stabilization needs to be studied. Preliminary data from our recent single-center study confirmed the feasibility of using V-PPV for resuscitation of extremely premature babies and indicated its potential superiority with a 28% decrease in the need for intubation compared to historical use of T-piece. This promising innovation may enhance outcomes for these vulnerable infants by refining the way we provide respiratory support in their critical first moments. The research objective is to compare the clinical outcomes of extremely premature infants receiving manual T-piece versus V-PPV during immediate post-birth stabilization. The primary aim is to evaluate the impact of V-PPV on major health complications or death. This study seeks to provide insights into improving the care and outcomes of these infants during a critical stage of transition from fetus to newborn.

Eligibility

Sex
ALL
Min age
25 Weeks
Max age
29 Weeks
Healthy volunteers
No
Inclusion Criteria:: * GA 25+0 to 28+6 weeks using the best available obstetrical estimate * Designated to receive full resuscitation, i.e., not pre-determined to receive only comfort care * Received PPV as determined by the resuscitation team during the first 10 minutes of birth Exclusion Criteria: * Outborn birth status * Resuscitation performed in unforeseen circumstances outside typical delivery room (e.g., emergency department, antenatal ward) * Known major congenital or chromosomal anomaly * Established spontaneous respiration without receipt of PPV

Primary outcome measure(s)

Trial sites (10)

FacilityCityRegionStatus
Cedars-Sinai Guerin Children's Los Angeles California Recruiting
Foothills Medical Centre Calgary Alberta Recruiting
Royal Alexandra Hospital Edmonton Alberta Recruiting
BC Children's and Women's Hospital Vancouver British Columbia Not Yet Recruiting
McMaster Children's Hospital Hamilton Ontario Recruiting
Children's Hospital at London Health Sciences Centre London Ontario Not Yet Recruiting
Mount Sinai Hospital Toronto Ontario Recruiting
Montreal Children's Hospital Montral Quebec Recruiting
CHU Sainte Justine Montreal Quebec Recruiting
Rigshospitalet Coppenhagen Copenhagen Denmark Not Yet Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06849596 on ClinicalTrials.gov ↗ ← All trials in Denmark