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Pediatric Difficult Intubation (3V-L DL)

I

International Institute of Rescue Research and Education

Status

Unknown

Conditions

Intubation
Cardiac Arrest

Treatments

Device: Vividtrac
Device: MIL

Study type

Interventional

Funder types

Other

Identifiers

NCT02295670
ETI/2014/51

Details and patient eligibility

About

Endotracheal intubation (ETI) is perceived as the optimal method of providing and maintaining a clear and secure airway. The 2010 European Resuscitation Council (ERC) guidelines emphasized the importance of minimal interruption during cardiopulmonary resuscitation (CPR). These guidelines also suggest that skilled operators should be able to secure the airway without interrupting chest compression. The aim of the study was to compare time and success rates of the Vividtrac video-laryngoscope and the Miller laryngoscope for emergency intubation during simulated pediatric CPR.

Enrollment

180 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Give voluntary consent to participate in the study
  • Paramedic student

Exclusion criteria

  • Not meet the above criteria
  • Wrist or Low back diseases

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

180 participants in 2 patient groups

Endotracheal intubation without chest compressions
Experimental group
Description:
Endotracheal intubation of mannikin during resuscitation without chest compressions.
Treatment:
Device: Vividtrac
Device: MIL
Endotracheal intubation with uninterrupted chest compressions
Experimental group
Description:
Endotracheal intubation of 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: Vividtrac
Device: MIL

Trial contacts and locations

1

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Central trial contact

Lukasz Szarpak

Data sourced from clinicaltrials.gov

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