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
About this trial
This is an interventional treatment trial for Cardiac Arrest focused on measuring intubation, child, resuscitation, simulation, Endotracheal
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
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
NCT ID
NCT02289677
First Posted
November 9, 2014
Last Updated
November 12, 2014
Sponsor
International Institute of Rescue Research and Education
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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