Actively Recruiting

Phase Not Applicable
Age: 0 - 19Years
All Genders
NCT06085326

Smart Checklist Implementation for Pediatric Tracheal Intubations in the ICU- Multicenter Study

Led by Children's Hospital of Philadelphia · Updated on 2025-10-20

3000

Participants Needed

6

Research Sites

260 weeks

Total Duration

On this page

Sponsors

C

Children's Hospital of Philadelphia

Lead Sponsor

A

Agency for Healthcare Research and Quality (AHRQ)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The purpose of the study is to implement a patient-provider dyad tailored, Electronic Health Record (EHR)-informed, digitized Smart Checklist as a Quality Improvement (QI) intervention to support bedside clinician teams to reduce Adverse Airway Outcomes (AAO) across 6 diverse pediatric intensive care units (ICUs).

CONDITIONS

Official Title

Smart Checklist Implementation for Pediatric Tracheal Intubations in the ICU- Multicenter Study

Who Can Participate

Age: 0 - 19Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • All patients intubated in the pediatric intensive care unit (PICU) at participating sites
Not Eligible

You will not qualify if you...

  • Endotracheal tube exchanges, as this is considered a different procedure

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 6 locations

1

University of Arkansas

Little Rock, Arkansas, United States, 72205

Actively Recruiting

2

Emory University

Atlanta, Georgia, United States, 30322

Actively Recruiting

3

University of Nebraska Medical Center

Omaha, Nebraska, United States, 68198

Actively Recruiting

4

Akron Children's Hospital

Akron, Ohio, United States, 44308

Actively Recruiting

5

Hasbro Children's Hospital

Providence, Rhode Island, United States, 02903

Actively Recruiting

6

University of Virginia

Charlottesville, Virginia, United States, 22903

Actively Recruiting

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Research Team

A

Akira Nishisaki, MD, MSCE

CONTACT

H

Hayley Buffman, MPH

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

PREVENTION

Number of Arms

2

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