Working…
COVID-19 is an emerging, rapidly evolving situation.
Get the latest public health information from CDC: https://www.coronavirus.gov.

Get the latest research information from NIH: https://www.nih.gov/coronavirus.
ClinicalTrials.gov
ClinicalTrials.gov Menu

Pediatric Intubation Among Nursing

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT02291640
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 video laryngoscope and direct laryngoscope for the emergency intubation with an immobilized cervical spine in a standardized pediatric manikin model.

Condition or disease Intervention/treatment Phase
Cardiac Arrest Intubation, Endotracheal Device: MIL Device: CoPilot Not Applicable

Layout table for study information
Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 130 participants
Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Coparison of Miller and CoPilot Laryngoscopes for Intubation by Nurses During Child Chest Compression. A Manikin Study
Study Start Date : November 2014
Estimated Primary Completion Date : December 2014
Estimated Study Completion Date : December 2014

Arm Intervention/treatment
Experimental: Child ETI with chest compressions
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: MIL
direct laryngoscopy
Other Name: Miller laryngoscope

Device: CoPilot
video laryngoscopy
Other Name: CoPilot VideoLaryngoscope

Experimental: Child ETI without chest compressions
Endotracheal intubation of child mannikin during resuscitation without chest compressions.
Device: MIL
direct laryngoscopy
Other Name: Miller laryngoscope

Device: CoPilot
video laryngoscopy
Other Name: CoPilot VideoLaryngoscope




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


Secondary Outcome Measures :
  1. Time to intubation [ Time Frame: 1 day ]
    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.If the examinee failed at all attempts, the case was excluded from the time calculations.


Other Outcome Measures:
  1. Cormack-Lehan scale [ Time Frame: 1 day ]
    self reported Cormack-Lehan scale during intubation



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
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 nursing

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): NCT02291640


Contacts
Layout table for location contacts
Contact: Andrzej Kurowski +48500186225 andrzejkurowski987@gmail.com
Contact: Lukasz Szarpak +48500186225 lukasz.szarpak@gmail.com

Locations
Layout table for location information
Poland
International Institute of Rescue Research and Education Recruiting
Warsaw, Masovia, Poland, 03-122
Contact: Lukasz Szarpak    +48500186225    lukasz.szarpak@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
Layout table for investigator information
Principal Investigator: Lukasz Szarpak Institute of Cardiology
Layout table for additonal information
Responsible Party: Lukasz Szarpak, Institute of Cardiology, Warsaw, Poland
ClinicalTrials.gov Identifier: NCT02291640    
Other Study ID Numbers: ETI/2014/16
First Posted: November 14, 2014    Key Record Dates
Last Update Posted: November 14, 2014
Last Verified: November 2014
Additional relevant MeSH terms:
Layout table for MeSH terms
Heart Arrest
Heart Diseases
Cardiovascular Diseases