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Pediatric Intubation With Difficult Airway

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ClinicalTrials.gov Identifier: NCT02291627
Recruitment Status : Unknown
Verified November 2014 by Lukasz Szarpak, Institute of Cardiology, Warsaw, Poland.
Recruitment status was:  Recruiting
First Posted : November 14, 2014
Last Update Posted : November 14, 2014
Sponsor:
Information provided by (Responsible Party):
Lukasz Szarpak, Institute of Cardiology, Warsaw, Poland

Brief Summary:
The aim of this study was to compare time, success rates of different video laryngoscopes for the emergency intubation with an immobilized cervical spine in a standardized pediatric manikin model.

Condition or disease Intervention/treatment Phase
Trauma Intubation, Endotracheal Device: MAC Device: Coopdech Device: AirTraq Not Applicable

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 120 participants
Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Comparison of the Macintosh, Coopdech and AirTraq Laryngoscopes Using a Rigid Neck Collar in Pediatric Patients With Simulated Difficult Laryngoscopy.
Study Start Date : November 2014
Estimated Primary Completion Date : December 2014
Estimated Study Completion Date : December 2014

Arm Intervention/treatment
Experimental: intubation with immobilized cervical spine
endotracheal intubation with immobilized cervical spine
Device: MAC
direct laryngoscopy
Other Name: Macintosh Laryngoscope

Device: Coopdech
Video laryngoscopy
Other Name: Coopdech Video Lartyngoscope Portable VLP-100

Device: AirTraq
optical laryngoscopy




Primary Outcome Measures :
  1. Success of intubation [ Time Frame: 1 day ]
    effectiveness of first, second and third intubation attempts and overall effectiveness of intubation by participants


Secondary Outcome Measures :
  1. Intubation time [ Time Frame: 1 day ]
    time in seconds required for a successful intubation attempt

  2. Cormack-Lehane grading [ Time Frame: 1 day ]
    self-reported percentage the vocal cord visualization using the Cormack-Lehane grading (grade 1-4)



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 65 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Give voluntary consent to participate in the study
  • minimum 1 year of work experience in emergency medicine
  • experienced emergency medical personnel (physicians, nurses, paramedics)

Exclusion Criteria:

  • Not meet the above criteria
  • Wrist or Low back diseases

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02291627


Contacts
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Contact: Andrzej Kurowski +48500186225 andrzejkurowski987@gmail.com

Locations
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Poland
International Institute of Rescue Research and Education Recruiting
Warsaw, Masovia, Poland, 03-122
Contact: Lukasz Czyżewski    +48500186225    rn.czyzewski@gmail.com   
Principal Investigator: Lukasz Szarpak         
Sub-Investigator: Andrzej Kurowski         
Sub-Investigator: Lukasz Czyżewski         
Sponsors and Collaborators
International Institute of Rescue Research and Education
Investigators
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Principal Investigator: Lukasz Szarpak Institute of Cardiology
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Responsible Party: Lukasz Szarpak, Institute of Cardiology, Warsaw, Poland
ClinicalTrials.gov Identifier: NCT02291627    
Other Study ID Numbers: ETI/2014/15
First Posted: November 14, 2014    Key Record Dates
Last Update Posted: November 14, 2014
Last Verified: November 2014