- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02074072
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
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Materials
- Sim Mom manikin (Laerdal, Stavanger, Norway)
- Stryker ST104-747(Transport stretcher®, 760 x 2110 mm, 228 kg, Stryker Co., Kalamazoo, Michigan, US)
- LUCAS Chest Compression System( LUCAS Chest Compression System, Physio-Control/Jolife AB)
- 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
-
-
-
Seoul, Korea, Republic of, 133792
- Hanyang University Seoul Hospital
-
-
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:
The wedges are made of aluminium
Other Names:
|
|
Experimental: Videolaryngoscope-1
Glidescope
|
The wedges are made of aluminium
Other Names:
The wedges are made of aluminium
Other Names:
|
|
Experimental: Videolaryngoscope-2
Airwayscope
|
The wedges are made of aluminium
Other Names:
The wedges are made of aluminium
Other Names:
|
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
|
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
|
|
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- HYI-14-004-1
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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