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Suspended Not applicable Interventional

Pediatric Prehospital Airway Resuscitation Trial

ClinicalTrials.gov ID: NCT06364280

Public ClinicalTrials.gov record NCT06364280. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 6, 2026, 5:47 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study is a Phase 3, multi-center, Bayesian Adaptive Sequential Platform Trial testing the effectiveness of different prehospital airway management strategies in the care of critically ill children. Emergency Medical Services (EMS) agencies affiliated with the Pediatric Emergency Care Applied Research Network (PECARN) will participate in the trial. The study interventions are strategies of prehospital airway management: \[BVM-only\], \[BVM followed by SGA\] and \[BVM followed by ETI\]. The primary outcome is 30-day ICU-free survival. The trial will be organized and executed in two successive stages. In Stage I of the trial, EMS personnel will alternate between two strategies: \[BVM-only\] or \[BVM followed by SGA\]. The \[winner of Stage I\] will advance to Stage II based upon results of Bayesian interim analyses. In Stage II of the trial, EMS personnel will alternate between \[BVM followed by ETI\] vs. \[Winner of Stage I\].

Study identification

NCT ID
NCT06364280
Recruitment status
Suspended
Study type
Interventional
Phase
Not applicable
Lead sponsor
Ohio State University
Other
Enrollment
3,000 participants

Conditions and interventions

Eligibility (public fields only)

Age range
24 Hours to 17 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 19, 2024
Primary completion
Aug 30, 2029
Completion
Sep 29, 2029
Last update posted
Apr 6, 2026

2024 – 2029

United States locations

U.S. sites
10
U.S. states
9
U.S. cities
10
Facility City State ZIP Site status
University of Airzona Tucson Arizona 85721
Harbor-University of California Los Angeles Medical Center Los Angeles California 90509
University of California Davis Sacramento California 95817
University of Colordao Aurora Colorado 80045
Children's National Hospital Washington D.C. District of Columbia 20010
Indiana University Indianapolis Indiana 46202
Mecklenburg County Emergency Medical Services Charlotte North Carolina 28208
Nationwide Children's Hospital Columbus Ohio 43205
Dell Medical School, University of Texas at Austin Austin Texas 78712
Medical College of Wisconsin Milwaukee Wisconsin 53226

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06364280, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 6, 2026 · Synced Sep 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06364280 live on ClinicalTrials.gov.

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