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Pediatric Intubation During Resuscitation

NCT02277405 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 150

Last updated 2014-10-29

No results posted yet for this study

Summary

The aim of the study was to compare time and success rates of four intubation devices in a cardiopulmonary scenario with and without chest compressions with a standardized pediatric manikin model.

Conditions

  • Intubation
  • Resuscitation

Interventions

DEVICE

Shikani Optical Stylet

Optical intubation

DEVICE

Endoeye Flexible Intubation (LF-V)

endoscopy intubation

Sponsors & Collaborators

  • International Institute of Rescue Research and Education

    lead OTHER

Principal Investigators

  • Lukasz Szarpak · National Institute of Cardiology, Warsaw, Poland

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-10-31
Primary Completion
2014-11-30
Completion
2014-11-30

Countries

  • Poland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02277405 on ClinicalTrials.gov