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VIDEO: Video-laryngoscopy During Chest Compression

Sponsor
International Institute of Rescue Research and Education (Other)
Overall Status
Unknown status
CT.gov ID
NCT02293226
Collaborator
(none)
150
Enrollment
1
Location
2
Arms
30
Duration (Days)
152.2
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Device: CoopDech
  • Device: CoPilot
  • Device: Intubrite
  • Device: Vividtrack
 N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
150 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Comparison of Four Video-laryngoscopes During Pediatric Intubation During Simulated Resuscitation
Study Start Date :
Nov 1, 2014
Anticipated Primary Completion Date :
Nov 1, 2014
Anticipated Study Completion Date :
Dec 1, 2014

Arms and Interventions

Arm Intervention/Treatment
Experimental: Child ETI with chest compressions

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.).

Device: CoopDech
Video-laryngoscopy 1
Other Names:
  • Coopdech Video Laryngoscope Portable VLP-100

    • Device: CoPilot
    video-laryngoscopy 2
    Other Names:
  • CoPilot VideoLaryngoscope

    • Device: Intubrite
    Video-laryngoscopy 3
    Other Names:
  • Intubrite Video Laryngoscope System VLS 6600

    • Device: Vividtrack
    video-laryngoscopy 4
    Experimental: Infant ETI with chest compressions

    endotracheal intubation (ETI) during infant mannikin resuscitation with uninterrupted chest compressions

    Device: CoopDech
    Video-laryngoscopy 1
    Other Names:
  • Coopdech Video Laryngoscope Portable VLP-100

    • Device: CoPilot
    video-laryngoscopy 2
    Other Names:
  • CoPilot VideoLaryngoscope

    • Device: Intubrite
    Video-laryngoscopy 3
    Other Names:
  • Intubrite Video Laryngoscope System VLS 6600

    • Device: Vividtrack
    video-laryngoscopy 4

    Outcome Measures

    Primary Outcome Measures

    1. Time to intubation [1 day]

      time from insertion of the blade to the first manual ventilation of the manikin´s lungs. If time of intubation is over than 60 seconds, attempt was recognized as failure.

    Secondary Outcome Measures

    1. Success of intubation [1 day]

      effectiveness of the first, second and third intubation attempts and overall effectiveness of intubation by participants using four intubation devices. If the examinee failed at all attempts, the case was excluded from the time calculations.

    2. Cormack-Lehan scale [1 day]

      self reported Cormack-Lehan scale during intubation

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 65 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    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

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 International Institute of Rescue Research and Education Warsaw Masovia Poland 03-122

    Sponsors and Collaborators

    • International Institute of Rescue Research and Education

    Investigators

    • Principal Investigator: Lukasz Szarpak, Institute of Cardiology

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Lukasz Szarpak, Lukasz Szarpak, Institute of Cardiology, Warsaw, Poland
    ClinicalTrials.gov Identifier:
    NCT02293226
    Other Study ID Numbers:
    • ETI/2014/19
    First Posted:
    Nov 18, 2014
    Last Update Posted:
    Nov 18, 2014
    Last Verified:
    Nov 1, 2014
    Additional relevant MeSH terms:
    Heart Arrest

    Study Results

    No Results Posted as of Nov 18, 2014