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NCT02997488 Clinical Trial

Comparison of Routine Endotracheal Intubation With McGrath Videolaryngoscope and Pentax AirwayScope

Intubation Clinical Trial

Official title:
Comparison of Routine Endotracheal Intubation With McGrath Videolaryngoscope and Pentax AirwayScope

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02997488
Other study ID # AJIRB-DEV-OBS-16-473
Secondary ID
Status Completed
Phase N/A
First received December 14, 2016
Last updated June 14, 2017
Start date February 9, 2017
Est. completion date June 14, 2017

Study information
Verified date June 2017
Source Ajou University School of Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Recently many kinds of indirect videolaryngoscopes were developed. These videolaryngoscopes provide easier intubation, help intubation difficulty, are used good tool for education. McGrath Videolaryngoscope and Pentax AirwayScope are kinds of these videolaryngoscopes.

The purpose of this study is to compare of routine endotracheal intubation with McGrath Videolaryngoscope and Pentax AirwayScope by means of providing better laryngeal view, easier and faster intubation.

Recruitment information / eligibility
Status Completed
Enrollment 140
Est. completion date June 14, 2017
Est. primary completion date June 14, 2017
Accepts healthy volunteers No
Gender All
Age group 19 Years to 65 Years
Eligibility Inclusion Criteria:

- an American Society of Anesthesiologists physical status (ASA) 1 or 2

Exclusion Criteria:

- a suspected difficult airway (Mallampati score ?)

- known cervical spine injury

- required rapid sequence induction

- emergency operation

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• Pentax Airwayscope
intubation using Pentax Airwayscope
• McGrath Videolaryngoscope
intubation using McGrath Videolaryngoscope

Locations
Country Name City State
Korea, Republic of Ajou University School of Medicine Suwon

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 Time to intubation from entering of blade between incisors to appearance of first end tidal CO2 curve using capnograph 10 minutes around intubation
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