Pediatric Intubation During CPR
ETICPR
Comparison of the Atmos Scope, the Coopdech and the AirTraq in Pediatric Patients During Resuscitation. Randomized Crossover Manikin Trial
1 other identifier
interventional
100
0 countries
N/A
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Nov 2014
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 1, 2014
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2014
CompletedStudy Completion
Last participant's last visit for all outcomes
November 1, 2014
CompletedFirst Submitted
Initial submission to the registry
November 9, 2014
CompletedFirst Posted
Study publicly available on registry
November 13, 2014
CompletedNovember 13, 2014
November 1, 2014
Same day
November 9, 2014
November 12, 2014
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Success of intubation
effectiveness of first, second and third intubation attempts and overall effectiveness of intubation by participants using two intubation devices
1 day
Secondary Outcomes (3)
Intubation time
1 day
POGO score
1 day
Cormack-Lehane grading
1 day
Study Arms (1)
Intubation during chest compression
EXPERIMENTALIntubation during mannequin chest compressions. Chest compression was performed using LUCAS-2 (Physio-Control, Redmond, WA, USA).
Interventions
Video-laryngoscopy 1
Video-laryngoscopy-1
Eligibility Criteria
You may qualify if:
- Give voluntary consent to participate in the study
- minimum 1 year of work experience in emergency medicine
- experienced emergency medical personnel (physicians, nurses, paramedics)
You may not qualify if:
- Not meet the above criteria
- Wrist or Low back diseases
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Lukasz Szarpak
Institute of Cardiology
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Lukasz Szarpak
Study Record Dates
First Submitted
November 9, 2014
First Posted
November 13, 2014
Study Start
November 1, 2014
Primary Completion
November 1, 2014
Study Completion
November 1, 2014
Last Updated
November 13, 2014
Record last verified: 2014-11