Effectiveness of Child Intubation
First Comparison of the /Intubrite VideoLaryngoscope System Versus the Miller Laryngoscope for Intubations by Non-anaesthetists: a Manikin Study.
1 other identifier
interventional
100
1 country
1
Brief Summary
We hypothesized that the Intubrite Video Laryngoscope System VLS 6600 is beneficial for intubation of pediatric manikins while performing CPR. In the current study, we compared effectiveness of the Intubrite and MIL laryngoscopes in child resuscitation with and without CC.
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
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
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 10, 2014
CompletedFirst Posted
Study publicly available on registry
November 13, 2014
CompletedNovember 13, 2014
November 1, 2014
Same day
November 10, 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
1 day
Secondary Outcomes (3)
Intubation time
1 day
POGO score
1 day
Cormack-Lehane grading
1 day
Study Arms (2)
Intubation without chest compressions
EXPERIMENTALEndotracheal intubation of pediatric mannikin during resuscitation without chest compressions.
Intubation with uninterrupted chest compressions
EXPERIMENTALEndotracheal intubation of pediatric 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
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 (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
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
- Institute of Cardiology, Warsaw, Poland
Study Record Dates
First Submitted
November 10, 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