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Video-laryngoscopy During Chest Compression (VIDEO)

I

International Institute of Rescue Research and Education

Status

Unknown

Conditions

Intubation, Endotracheal
Cardiac Arrest

Treatments

Device: Intubrite
Device: CoopDech
Device: Vividtrack
Device: CoPilot

Study type

Interventional

Funder types

Other

Identifiers

NCT02293226
ETI/2014/19

Details and patient eligibility

About

The investigators will compare the success rates and time to successful intubation of endotracheal intubation during simulated pediatric and infant resuscitation with and without chest compression using four different video-laryngoscopes.

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 nursing

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)

150 participants in 2 patient groups

Child ETI with chest compressions
Experimental group
Description:
endotracheal intubation (ETI) during child mannikin 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: CoPilot
Device: Vividtrack
Device: CoopDech
Device: Intubrite
Infant ETI with chest compressions
Experimental group
Description:
endotracheal intubation (ETI) during infant mannikin resuscitation with uninterrupted chest compressions
Treatment:
Device: CoPilot
Device: Vividtrack
Device: CoopDech
Device: Intubrite

Trial contacts and locations

1

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Central trial contact

Andrzej Kurowski

Data sourced from clinicaltrials.gov

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