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Pediatric Intubation During Resuscitation (PIDR)

I

International Institute of Rescue Research and Education

Status

Unknown

Conditions

Intubation
Resuscitation

Treatments

Device: Endoeye Flexible Intubation (LF-V)
Device: Shikani Optical Stylet

Study type

Interventional

Funder types

Other

Identifiers

NCT02277405
ETI/2014/04

Details and patient eligibility

About

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.

Full description

Emergency airway management during resuscitation is a critical skill in emergency medicine. According to the European Resuscitation Council (ERC) guidelines for resuscitation 2010 , endotracheal intubation (ETI) is considered the gold standard during resuscitation.

Enrollment

150 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • give voluntary consent to participate in the study
  • minimum 1 year of work experience in emergency medicine
  • experienced emergency medical personnel (paramedics, nurses, physicians)

Exclusion criteria

  • not meet the above criteria
  • wrist or low back diseases

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

150 participants in 2 patient groups

Intubation without chest compressions
Experimental group
Description:
Endotracheal intubation of pediatric mannikin during resuscitation without chest compressions.
Treatment:
Device: Endoeye Flexible Intubation (LF-V)
Device: Shikani Optical Stylet
Intubation with uninterrupted chest compressions
Experimental group
Description:
Endotracheal intubation of pediatric mannikin during resuscitation with uninterrupted chest compressions. In order to simulate the difficulties associated with intubation during uninterrupted chest compressions, CPR was performed by using LUCAS-2 (Physio-Control, Redmond, WA, U.S.).
Treatment:
Device: Endoeye Flexible Intubation (LF-V)
Device: Shikani Optical Stylet

Trial contacts and locations

1

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Central trial contact

Lukasz Czyzewski

Data sourced from clinicaltrials.gov

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