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

March 17, 2014 updated by: Jaehoon Oh, Hanyang University
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.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

21

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 60 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Basic Science
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: a 65 cm bed height
1) Bed height : approximately 65cm (Lowest)
Device: Macintosh laryngoscope
Direct Laryngoscope
Device: Glidescope
Videolaryngoscope-1
Device: Airwayscope
Videolaryngoscope-2
Experimental: a 95cm bed height
2) Bed height : approximately 95cm (highest)
Device: Macintosh laryngoscope
Direct Laryngoscope
Device: Glidescope
Videolaryngoscope-1
Device: Airwayscope
Videolaryngoscope-2

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
To measure a time to expose the glottis view with a laryngoscope
Time Frame: 1 day
1 day
To measure a time to intubate the tube with a laryngoscope
Time Frame: 1 day
1 day
To estimate the success rate of Intubation
Time Frame: 1 day
" Failure " means that tube is inserted in esophagus and the time is over than 120 seconds
1 day

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
To assess the grade for the glottis view with a laryngoscopy
Time Frame: 1 day
Using the Cormack-Lehane Grade system
1 day

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
To assess the preference for a type of laryngoscopes
Time Frame: 1 day
The participant select the type of a laryngoscope if he/she performs the endotracheal intubation under the experimental situation again.
1 day

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Hanyang University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

March 1, 2014

Primary Completion (Actual)

March 1, 2014

Study Completion (Actual)

March 1, 2014

Study Registration Dates

First Submitted

February 20, 2014

First Submitted That Met QC Criteria

February 27, 2014

First Posted (Estimate)

February 28, 2014

Study Record Updates

Last Update Posted (Estimate)

March 18, 2014

Last Update Submitted That Met QC Criteria

March 17, 2014

Last Verified

March 1, 2014

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Intubation with a bed height

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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