- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02074098
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
-
-
-
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: a 65 cm bed height
1) Bed height : approximately 65cm (Lowest)
|
Direct Laryngoscope
Videolaryngoscope-1
Videolaryngoscope-2
|
Experimental: a 95cm bed height
2) Bed height : approximately 95cm (highest)
|
Direct Laryngoscope
Videolaryngoscope-1
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
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
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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