Endotracheal Intubation Using Three Laryngoscopes in Maternal Cardiac Arrest: a Manikin Simulation Study

March 20, 2014 updated by: Lee Sang Hyun, Hanyang University Seoul Hospital

Comparison of Glidescope, Pentax-AWS and Macintosh Laryngoscope for Intubation During Chest Compression in 15-30 Degree Left-Lateral Tilt: A Manikin Simulation Study of Maternal Cardiopulmonary Resuscitation

European Resuscitation Council (ERC) Guidelines for Resuscitation 2010 emphasize high quality chest compressions .They propose minor changes for pregnant women: manual left deviation of the uterus or a left-lateral incline of 15-30to alleviate pressure on the inferior vena cava. We will examine the performance of the Glidescope (GVL), the Pentax-AWS Airwayscope(AWS) and Macintosh laryngoscope (McL) for airway management during chest compressions on 15 and 30 degree left-lateral tilt (15 &30 LLT) custom-made hard wedges.

Study Overview

Detailed Description

Materials

  1. Sim Mom manikin (Laerdal, Stavanger, Norway)
  2. Stryker ST104-747(Transport stretcher®, 760 x 2110 mm, 228 kg, Stryker Co., Kalamazoo, Michigan, US)
  3. LUCAS Chest Compression System( LUCAS Chest Compression System, Physio-Control/Jolife AB)
  4. Backboard(450 ×600 ×10 mm, 3 kg Lifeline Plastic, Sung Shim Medical Co., Bucheon, Korea)

Study Type

Interventional

Enrollment (Actual)

19

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: Direct laryngoscope
Macintosh laryngoscope
The wedges are made of aluminium
Other Names:
  • Custom-made hard wedges
The wedges are made of aluminium
Other Names:
  • Custom-made hard wedges
Experimental: Videolaryngoscope-1
Glidescope
The wedges are made of aluminium
Other Names:
  • Custom-made hard wedges
The wedges are made of aluminium
Other Names:
  • Custom-made hard wedges
Experimental: Videolaryngoscope-2
Airwayscope
The wedges are made of aluminium
Other Names:
  • Custom-made hard wedges
The wedges are made of aluminium
Other Names:
  • Custom-made hard wedges

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Time to intubation
Time Frame: 1day
We will check the times from inserting blade to mouth to exposing vocal cord and from exposing vocal cord to first ambu-bagging.
1day
Success rate of intubation
Time Frame: 1day

Definition of failed intubation

  • Time to intubation is longer than 90 seconds.
  • Wrong placement of endotracheal tube (For example : Esophageal intubation etc.)
1day

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Laryngeal View during intubation
Time Frame: 1day
We will record the best laryngeal View during intubation. We will record according to the Cormack-Lehane Grade system.
1day
The preference for laryngoscopes
Time Frame: 1day
  1. The preference for laryngoscope regardless of tilting degree of wedges
  2. The preference for laryngoscope in 15 degree left-lateral tilt situation .
  3. The preference for laryngoscope in 30 degree left-lateral tilt situation . (Participants will select only 1 of 3 laryngoscopes and the preference will be displayed as histogram)
1day

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Sang hyun Lee, M.D, Hanyang University Seoul Hospital

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 25, 2014

First Submitted That Met QC Criteria

February 27, 2014

First Posted (Estimate)

February 28, 2014

Study Record Updates

Last Update Posted (Estimate)

March 21, 2014

Last Update Submitted That Met QC Criteria

March 20, 2014

Last Verified

March 1, 2014

More Information

Terms related to this study

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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