Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07419438

Supraglottic Airway for Resuscitation in Preemies

Supraglottic Airway Interface for Positive Pressure Ventilation During Delivery Room Resuscitation of Premature Infants: A Pilot Feasibility Trial

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
20 (estimated)
Sponsor
University of Pennsylvania · Academic / Other
Sex
All
Age
0 Days – 1 Day
Healthy volunteers
Not accepted

Summary

The goal of this single-arm intervention trial is to learn whether using a supraglottic airway (SA) as the primary interface for positive pressure ventilation (PPV) is feasible during delivery room resuscitation of premature infants. This study will be conducted in premature infants born between 29 0/7 and 33 6/7 weeks' gestation who require PPV at birth. The main question it aims to answer is: Is it feasible to use a supraglottic airway as the primary interface to provide effective PPV during delivery room resuscitation in 29 0/7 to 33 6/7 weeks' gestation premature infants? Participants will (1)Be screened prenatally and have informed consent obtained from the birth parent prior to delivery; (2)Be rescreened for eligibility on the day of delivery before receiving the study intervention; (3)Receive PPV using a supraglottic airway as the primary ventilation interface if resuscitation is required at birth; and (4)Have clinical and procedural data collected during delivery room resuscitation and for up to 24 hours after birth.

Conditions

Interventions

TypeNameDescription
OTHERSupraglottic AirwayUse of a supraglottic airway as the primary interface for delivery of positive pressure ventilation during neonatal resuscitation.

Timeline

Start date
2026-03-13
Primary completion
2026-06-01
Completion
2026-10-01
First posted
2026-02-19
Last updated
2026-04-17

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT07419438. Inclusion in this directory is not an endorsement.