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Pediatric Intubation During CPR (ETICPR)

Primary Purpose

Cardiac Arrest

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
ATMOS Scope
COOPDECH
AirTraq
Sponsored by
International Institute of Rescue Research and Education
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cardiac Arrest focused on measuring intubation, child, resuscitation, simulation, Endotracheal

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts 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 (physicians, nurses, paramedics)

Exclusion Criteria:

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

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    Intubation during chest compression

    Arm Description

    Intubation during mannequin chest compressions. Chest compression was performed using LUCAS-2 (Physio-Control, Redmond, WA, USA).

    Outcomes

    Primary Outcome Measures

    Success of intubation
    effectiveness of first, second and third intubation attempts and overall effectiveness of intubation by participants using two intubation devices

    Secondary Outcome Measures

    Intubation time
    time in seconds required for a successful intubation attempt
    POGO score
    self-reported percentage of glottis opening (POGO) score
    Cormack-Lehane grading
    self-reported percentage the vocal cord visualization using the Cormack-Lehane grading (grade 1-4)

    Full Information

    First Posted
    November 9, 2014
    Last Updated
    November 12, 2014
    Sponsor
    International Institute of Rescue Research and Education
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02289677
    Brief Title
    Pediatric Intubation During CPR
    Acronym
    ETICPR
    Official Title
    Comparison of the Atmos Scope, the Coopdech and the AirTraq in Pediatric Patients During Resuscitation. Randomized Crossover Manikin Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    November 2014
    Overall Recruitment Status
    Unknown status
    Study Start Date
    November 2014 (undefined)
    Primary Completion Date
    November 2014 (Anticipated)
    Study Completion Date
    November 2014 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    International Institute of Rescue Research and Education

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    We hypothesized that the video-laryngoscopes are beneficial for intubation of pediatric manikins while performing CPR. In the current study, we compared effectiveness of two video-laryngoscopes (the Coopdech video Laryngoscope portable VLp-100 and the Flexible Videoendoscope: ATMOS Scope) and optical-laryngoscope (the AirTraq) during resuscitation with uninterrupted chest compressions using an child manikin.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Cardiac Arrest
    Keywords
    intubation, child, resuscitation, simulation, Endotracheal

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Crossover Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    100 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Intubation during chest compression
    Arm Type
    Experimental
    Arm Description
    Intubation during mannequin chest compressions. Chest compression was performed using LUCAS-2 (Physio-Control, Redmond, WA, USA).
    Intervention Type
    Device
    Intervention Name(s)
    ATMOS Scope
    Other Intervention Name(s)
    ATMOS Scope Flexible Videoendoscope
    Intervention Description
    Video-laryngoscopy 1
    Intervention Type
    Device
    Intervention Name(s)
    COOPDECH
    Other Intervention Name(s)
    COOPDECH Video Laryngoscope Portable VLP-100
    Intervention Description
    Video-laryngoscopy-1
    Intervention Type
    Device
    Intervention Name(s)
    AirTraq
    Intervention Description
    Optical-laryngoscopy
    Primary Outcome Measure Information:
    Title
    Success of intubation
    Description
    effectiveness of first, second and third intubation attempts and overall effectiveness of intubation by participants using two intubation devices
    Time Frame
    1 day
    Secondary Outcome Measure Information:
    Title
    Intubation time
    Description
    time in seconds required for a successful intubation attempt
    Time Frame
    1 day
    Title
    POGO score
    Description
    self-reported percentage of glottis opening (POGO) score
    Time Frame
    1 day
    Title
    Cormack-Lehane grading
    Description
    self-reported percentage the vocal cord visualization using the Cormack-Lehane grading (grade 1-4)
    Time Frame
    1 day

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Give voluntary consent to participate in the study minimum 1 year of work experience in emergency medicine experienced emergency medical personnel (physicians, nurses, paramedics) Exclusion Criteria: Not meet the above criteria Wrist or Low back diseases
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Lukasz Szarpak
    Organizational Affiliation
    Institute of Cardiology
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Learn more about this trial

    Pediatric Intubation During CPR

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