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

• Sponsor: Hanyang University (Other)
• Overall Status: Completed
• CT.gov ID: NCT02074098
• Collaborator: (none)
• Enrollment: 21
• Location: 1
• Arms: 2

Study Details

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.

Condition or Disease	Intervention/Treatment	Phase
Tracheal Intubation; Cardiac Arrest	Device: Macintosh laryngoscope; Device: Glidescope; Device: Airwayscope	N/A

Study Design

• Study Type: Interventional
• Actual Enrollment: 21 participants
• Allocation: Randomized
• Intervention Model: Crossover Assignment
• Masking: Single (Outcomes Assessor)
• Primary Purpose: Basic Science
• Study Start Date: Mar 1, 2014
• Actual Primary Completion Date: Mar 1, 2014
• Actual Study Completion Date: Mar 1, 2014

Arms and Interventions

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

Outcome Measures

Primary Outcome Measures

1. To measure a time to expose the glottis view with a laryngoscope [1 day]

2. To measure a time to intubate the tube with a laryngoscope [1 day]

3. To estimate the success rate of Intubation [1 day]

   " Failure " means that tube is inserted in esophagus and the time is over than 120 seconds

Secondary Outcome Measures

1. To assess the grade for the glottis view with a laryngoscopy [1 day]

   Using the Cormack-Lehane Grade system

Other Outcome Measures

1. To assess the preference for a type of laryngoscopes [1 day]

   The participant select the type of a laryngoscope if he/she performs the endotracheal intubation under the experimental situation again.

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years to 60 Years
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: Yes

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

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Hanyang University Seoul Hospital	Seoul		Korea, Republic of	133792

Sponsors and Collaborators

• Hanyang University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Jaehoon Oh, Clinical fellow, Hanyang University
• ClinicalTrials.gov Identifier: NCT02074098
• Other Study ID Numbers: Intubation with a bed height
• First Posted: Feb 28, 2014
• Last Update Posted: Mar 18, 2014
• Last Verified: Mar 1, 2014

• Keywords provided by Jaehoon Oh, Clinical fellow, Hanyang University: intubation; Cardiopulmonary resuscitation; Manikin study
• Additional relevant MeSH terms: Heart Arrest

Study Results

No Results Posted as of Mar 18, 2014