Pediatric Intubation by Nurses
NURS_ETI
Comparison of Pentax-AWS Airwayscope, Intubrite, AirTraq and Miller Laryngoscope for Tracheal Intubation by Nurses During Chest Compression in a Pediatric Manikin: A Randomised Crossover Trial.
1 other identifier
interventional
150
1 country
1
Brief Summary
The purpose of this study was to compare the Pentax AWS, Intubrite and AirTraq to Miller laryngoscope during pediatric resuscitation with and without chest compressions.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Nov 2014
Shorter than P25 for not_applicable
1 active site
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
CompletedFirst Submitted
Initial submission to the registry
November 16, 2014
CompletedFirst Posted
Study publicly available on registry
November 19, 2014
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2014
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2014
CompletedNovember 19, 2014
November 1, 2014
1 month
November 16, 2014
November 16, 2014
Conditions
Outcome Measures
Primary Outcomes (1)
Time to intubation
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.
1 day
Secondary Outcomes (3)
Success of intubation
1 day
VAS score
1 day
Cormack-Lehan scale
1day
Study Arms (2)
Child ETI withoutchest compressions
EXPERIMENTALEndotracheal intubation of pediatric mannikin during resuscitation without chest compressions.
Child ETI with chest compressions
EXPERIMENTALEndotracheal intubation of mannikin during 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.).
Interventions
Video-laryngoscopy 1
Video-laryngoscopy 2
Optical-laryngoscopy
Direct-laryngoscopy
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 - nurses
You may not qualify if:
- not meet the above criteria
- wrist or low back diseases
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
International Institute of Rescue Research and Education
Warsaw, Masovia, 03-122, Poland
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Lukasz Szarpak
Institute of Cardiology
Central Study Contacts
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 16, 2014
First Posted
November 19, 2014
Study Start
November 1, 2014
Primary Completion
December 1, 2014
Study Completion
December 1, 2014
Last Updated
November 19, 2014
Record last verified: 2014-11