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EIDR: Endotracheal Intubation During Resuscitation

Sponsor
International Institute of Rescue Research and Education (Other)
Overall Status
Unknown status
CT.gov ID
NCT02286323
Collaborator
(none)
130
Enrollment
1
Location
2
Arms

Study Details

Study Description

Brief Summary

We hypothesized that the BONFILS is beneficial for intubation of manikins while performing CPR. In the current study we compared the performance of the BONFILS and the Macintosh laryngoscopes with respect to their effectiveness and time to successful ETI during chest compression (CC) using an adult manikin.

Condition or Disease Intervention/Treatment Phase
  • Device: Bonfils
  • Device: Macintosh
 N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
130 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Can the Bonfils Intubation Fiberscope Rival the Macintosh Laryngoscope During Resuscitation With Uninterrupted Chest Compression?
Study Start Date :
Nov 1, 2014
Anticipated Primary Completion Date :
Nov 1, 2014
Anticipated Study Completion Date :
Nov 1, 2014

Arms and Interventions

Arm Intervention/Treatment
Experimental: Endotracheal intubation without chest compressions

Endotracheal intubation of mannikin during resuscitation without chest compressions.

Device: Bonfils
Bonfils Intubation Fiberoscope

Device: Macintosh
Direct laryngoscopy using Macintosh Laryngoscope
Experimental: Endotracheal intubation with uninterrupted chest compressions

Endotracheal 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.).

Device: Bonfils
Bonfils Intubation Fiberoscope

Device: Macintosh
Direct laryngoscopy using Macintosh Laryngoscope

Outcome Measures

Primary Outcome Measures

  1. Time to intubation [intraoperative]

    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.

Secondary Outcome Measures

  1. Success of intubation [intraoperative]

    effectiveness of the first, second and third intubation attempts and overall effectiveness of intubation by participants using four intubation devices. If the examinee failed at all attempts, the case was excluded from the time calculations.

  2. POGO score [1 day]

    self-reported percentage of glottis opening (POGO) score

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:

  • give voluntary consent to participate in the study

  • minimum 1 year of work experience in emergency medicine

  • experienced emergency medical personnel (paramedics, nurses, physicians)

Exclusion Criteria:

  • not meet the above criteria

  • wrist or low back diseases

Contacts and Locations

Locations

Site City State Country Postal Code
1 International Institute of Rescue Research and Education Warsaw Masovia Poland 04-628

Sponsors and Collaborators

  • International Institute of Rescue Research and Education

Investigators

  • Principal Investigator: Andrzej Kurowski, Institute of Cardiology

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Lukasz Szarpak, Lukasz Szarpak, Institute of Cardiology, Warsaw, Poland
ClinicalTrials.gov Identifier:
NCT02286323
Other Study ID Numbers:
  • ETI/2014/07
First Posted:
Nov 7, 2014
Last Update Posted:
Nov 10, 2014
Last Verified:
Nov 1, 2014
Keywords provided by Lukasz Szarpak, Lukasz Szarpak, Institute of Cardiology, Warsaw, Poland
Intubation, Endotracheal
Additional relevant MeSH terms:
Heart Arrest

Study Results

No Results Posted as of Nov 10, 2014