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NCT03677505 Clinical Trial

KoMAC Videolaryngoscope for Double-lumen Intubation

Intubation Clinical Trial

Official title:
Comparison of the KoMAC Videolaryngoscope With the Macintosh Laryngoscope for Double-lumen Intubation

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03677505
Other study ID # AJIRB-MED-OBS-18-286
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 5, 2018
Est. completion date March 2, 2020

Study information
Verified date March 2020
Source Ajou University School of Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

KoMAC videolaryngoscope is a portable intubating device with an angulated single-use blade of adjustable size and a liquid crystal display monitor mounted on top of the handle, which is similar in shape to the McGrath videolaryngoscope. The purpose of this study was to evaluate the efficacy of the KoMAC videolaryngoscope for double-lumen intubation regarding intubation time, laryngeal view and ease of intubation, compared to Macintosh laryngoscope.

Recruitment information / eligibility
Status Completed
Enrollment 60
Est. completion date March 2, 2020
Est. primary completion date February 27, 2020
Accepts healthy volunteers No
Gender All
Age group 19 Years to 65 Years
Eligibility Inclusion Criteria:

- patients scheduled for thoracic surgery requiring one lung ventilation

Exclusion Criteria:

- predicted difficult airway

- rapid sequence intubation

- cervical injury

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• KoMAC videolaryngoscope
Double lumen endotracheal intubation was performed with the KoMAC videolaryngoscope
• Macintosh Laryngoscope
Double lumen endotracheal intubation was performed with the Macintosh Laryngoscope

Locations
Country Name City State
Korea, Republic of Ajou University Hospital Suwon Gyeonggi-do

Sponsors (1)
Lead Sponsor Collaborator
Ajou University School of Medicine

Country where clinical trial is conducted

Korea, Republic of, 

Outcome
Type Measure Description Time frame Safety issue
Primary Intubation time Time interval between laryngoscope passing the teeth to the confirming of end tidal CO2 from 2 min after rocuronium injection to completion of intubation (time interval is about 120 seconds)
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