NCT02293226

Brief Summary

The investigators will compare the success rates and time to successful intubation of endotracheal intubation during simulated pediatric and infant resuscitation with and without chest compression using four different video-laryngoscopes.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
150

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Nov 2014

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

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

Completed
Same day until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2014

Completed
12 days until next milestone

First Submitted

Initial submission to the registry

November 13, 2014

Completed
5 days until next milestone

First Posted

Study publicly available on registry

November 18, 2014

Completed
13 days until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2014

Completed
Last Updated

November 18, 2014

Status Verified

November 1, 2014

Enrollment Period

Same day

First QC Date

November 13, 2014

Last Update Submit

November 17, 2014

Conditions

Cardiac ArrestIntubation, Endotracheal

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 (2)

  • Success of intubation

    1 day

  • Cormack-Lehan scale

    1 day

Study Arms (2)

Child ETI with chest compressions

EXPERIMENTAL

endotracheal intubation (ETI) during child mannikin 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.).

Device: CoopDechDevice: CoPilotDevice: IntubriteDevice: Vividtrack

Infant ETI with chest compressions

EXPERIMENTAL

endotracheal intubation (ETI) during infant mannikin resuscitation with uninterrupted chest compressions

Device: CoopDechDevice: CoPilotDevice: IntubriteDevice: Vividtrack

Interventions

CoopDechDEVICE

Video-laryngoscopy 1

Also known as: Coopdech Video Laryngoscope Portable VLP-100
Child ETI with chest compressionsInfant ETI with chest compressions
CoPilotDEVICE

video-laryngoscopy 2

Also known as: CoPilot VideoLaryngoscope
Child ETI with chest compressionsInfant ETI with chest compressions
IntubriteDEVICE

Video-laryngoscopy 3

Also known as: Intubrite Video Laryngoscope System VLS 6600
Child ETI with chest compressionsInfant ETI with chest compressions
VividtrackDEVICE

video-laryngoscopy 4

Child ETI with chest compressionsInfant ETI with chest compressions

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Give voluntary consent to participate in the study
  • Minimum 1 year of work experience in nursing

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

Location

MeSH Terms

Conditions

Heart Arrest

Condition Hierarchy (Ancestors)

Heart DiseasesCardiovascular Diseases

Study Officials

  • Lukasz Szarpak

    Institute of Cardiology

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Andrzej Kurowski

CONTACT

+48500186225andrzejkurowski987@gmail.com

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 13, 2014

First Posted

November 18, 2014

Study Start

November 1, 2014

Primary Completion

November 1, 2014

Study Completion

December 1, 2014

Last Updated

November 18, 2014

Record last verified: 2014-11

Locations

PL(1)