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NCT07419438 · ClinicalTrials.gov registry record · NA
Supraglottic Airway for Resuscitation in Preemies
A NA study of Respiratory Failure and Neonatal Resuscitation, sponsored by University of Pennsylvania.
- Recruiting
- Registry status
- NA
- Development phase
- 20
- Enrollment target
- 1
- Study location
NCT07419438: Recruiting NA study of Respiratory Failure and Neonatal Resuscitation, sponsored by University of Pennsylvania.
NCT07419438 is a NA study of Respiratory Failure and Neonatal Resuscitation that is actively recruiting participants, run by University of Pennsylvania. The registered enrollment target is 20 participants, below the 4,523-participant average among 40 other Respiratory Failure trials with a reported enrollment target (100% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT07419438, a NA study of Respiratory Failure and Neonatal Resuscitation, is actively recruiting participants, sponsored by University of Pennsylvania.
- RECRUITING
- Registry status
- NA
- Development phase
- 20 participants
- Enrollment target
- 1
- Study location
Study 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.
Primary Outcome
Feasibility defined as successful use of a supraglottic airway as the primary interface to deliver positive pressure ventilation for up to 10 minutes of life or until discontinuation of positive pressure ventilation, without need for immediate escalation to an alternative airway interface.
Conditions Studied
Interventions
- OTHER Supraglottic Airway
Study Locations (1)
Pennsylvania
- Hospital of the University of Pennsylvania - Philadelphia
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2026-02 |
| Est. Completion | 2026-10 |
| Phase | NA |
What NCT07419438 shows while recruiting
NCT07419438 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 4,523-participant average among 40 other Respiratory Failure trials with a reported enrollment target (100% lower).
The record links to 8 conditions, with Respiratory Failure appearing as the primary indexed condition, and to 1 intervention - of which Supraglottic Airway is the first listed.
NCT07419438 reports a single indexed study location in Pennsylvania.
Frequently Asked Questions
What is clinical trial NCT07419438 about?
NCT07419438 is a clinical study titled "Supraglottic Airway for Resuscitation in Preemies". 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 ...
What is the current status of trial NCT07419438?
This trial is currently recruiting. It is a NA study. The enrollment target is 20 participants. The study started on 2026-02. Estimated completion is 2026-10.
What conditions does trial NCT07419438 study?
This clinical trial studies the following conditions: Respiratory Failure, Neonatal Resuscitation, Supraglottic Airway, Delivery Room Resuscitation, Positive Pressure Ventilation.
What interventions are being tested in trial NCT07419438?
The interventions under investigation include: Supraglottic Airway (OTHER).
Who is sponsoring clinical trial NCT07419438?
This trial is sponsored by University of Pennsylvania, which has 1,423 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07419438 being conducted?
This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT07419438's enrollment target sits among peer trials
20 36th of 40 higher than 5 of 40 other Respiratory Failure trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Respiratory Failure trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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