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Endotracheal Intubation Using Macintosh Laryngoscope, Glidescope, Airwayscope During Chest Compression With Adjustment Height of a Bed

Primary Purpose

Tracheal Intubation, Cardiac Arrest

Status
Completed
Phase
Not Applicable
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Macintosh laryngoscope
Glidescope
Airwayscope
Sponsored by
Hanyang University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Tracheal Intubation focused on measuring intubation, Cardiopulmonary resuscitation, Manikin study

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Experience of Intubation > 50 times
  • Postgraduates year 1,2,3,4 and Emergency physicians in emergency department

Exclusion Criteria:

  • Wrist or low back disease

Sites / Locations

  • Hanyang University Seoul Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

a 65 cm bed height

a 95cm bed height

Arm Description

1) Bed height : approximately 65cm (Lowest)

2) Bed height : approximately 95cm (highest)

Outcomes

Primary Outcome Measures

To measure a time to expose the glottis view with a laryngoscope
To measure a time to intubate the tube with a laryngoscope
To estimate the success rate of Intubation
" Failure " means that tube is inserted in esophagus and the time is over than 120 seconds

Secondary Outcome Measures

To assess the grade for the glottis view with a laryngoscopy
Using the Cormack-Lehane Grade system

Full Information

First Posted
February 20, 2014
Last Updated
March 17, 2014
Sponsor
Hanyang University
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1. Study Identification

Unique Protocol Identification Number
NCT02074098
Brief Title
Endotracheal Intubation Using Macintosh Laryngoscope, Glidescope, Airwayscope During Chest Compression With Adjustment Height of a Bed
Study Type
Interventional

2. Study Status

Record Verification Date
March 2014
Overall Recruitment Status
Completed
Study Start Date
March 2014 (undefined)
Primary Completion Date
March 2014 (Actual)
Study Completion Date
March 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hanyang University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to determine whether a bed height make an effect to endotracheal intubation with Macintosh laryngoscope, Glidescope and Airwayscope during chest compressions in- hospital simulation cardiac arrest.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tracheal Intubation, Cardiac Arrest
Keywords
intubation, Cardiopulmonary resuscitation, Manikin study

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
21 (Actual)

8. Arms, Groups, and Interventions

Arm Title
a 65 cm bed height
Arm Type
Experimental
Arm Description
1) Bed height : approximately 65cm (Lowest)
Arm Title
a 95cm bed height
Arm Type
Experimental
Arm Description
2) Bed height : approximately 95cm (highest)
Intervention Type
Device
Intervention Name(s)
Macintosh laryngoscope
Intervention Description
Direct Laryngoscope
Intervention Type
Device
Intervention Name(s)
Glidescope
Intervention Description
Videolaryngoscope-1
Intervention Type
Device
Intervention Name(s)
Airwayscope
Intervention Description
Videolaryngoscope-2
Primary Outcome Measure Information:
Title
To measure a time to expose the glottis view with a laryngoscope
Time Frame
1 day
Title
To measure a time to intubate the tube with a laryngoscope
Time Frame
1 day
Title
To estimate the success rate of Intubation
Description
" Failure " means that tube is inserted in esophagus and the time is over than 120 seconds
Time Frame
1 day
Secondary Outcome Measure Information:
Title
To assess the grade for the glottis view with a laryngoscopy
Description
Using the Cormack-Lehane Grade system
Time Frame
1 day
Other Pre-specified Outcome Measures:
Title
To assess the preference for a type of laryngoscopes
Description
The participant select the type of a laryngoscope if he/she performs the endotracheal intubation under the experimental situation again.
Time Frame
1 day

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Experience of Intubation > 50 times Postgraduates year 1,2,3,4 and Emergency physicians in emergency department Exclusion Criteria: Wrist or low back disease
Facility Information:
Facility Name
Hanyang University Seoul Hospital
City
Seoul
ZIP/Postal Code
133792
Country
Korea, Republic of

12. IPD Sharing Statement

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Endotracheal Intubation Using Macintosh Laryngoscope, Glidescope, Airwayscope During Chest Compression With Adjustment Height of a Bed

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