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Clinical Trials/NCT04948294
NCT04948294
Completed
Not Applicable

Comparison of the Intubation Condition Between Using Two Types of Blade in Patients Receiving Tracheal Intubation Using Videolaryngoscope: Channeled Blade vs. Non-channeled Blade

Kyung Hee University Hospital at Gangdong1 site in 1 country118 target enrollmentAugust 22, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Intubation Complication
Sponsor
Kyung Hee University Hospital at Gangdong
Enrollment
118
Locations
1
Primary Endpoint
Intubation time
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The present study compares two different types of videolaryngoscope blade, which is a channeled and non-channeled blade. The purpose of the study is to investigate the effect of the type of videolaryngoscope blade on the intubation condition.

Detailed Description

In tracheal intubation for general anesthesia, one of the two types of the blade during a video laryngoscopy can be used, one is a channeled blade that has a channel for tracheal tube launching, the other is a non-channeled blade. In the present study, the outcomes by using two types of the videolaryngoscope blade such as the intubation condition, intubation time, first-pass rate, and the incidence of intubation-related complications were compared.

Registry
clinicaltrials.gov
Start Date
August 22, 2018
End Date
December 31, 2021
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Hyungseok Seo

Assistant Professor

Kyung Hee University Hospital at Gangdong

Eligibility Criteria

Inclusion Criteria

  • Patients receiving tracheal intubation for general anesthesia
  • Patients with physical status 1, 2, or 3 by American Society of Anesthesiologists Physical Status.

Exclusion Criteria

  • Body mass index \<18.5 kg/m2 or \>35 kg/m2
  • Patients with a history of airway surgery
  • Patients with increased risk of aspiration
  • Patients who have any pathology (polyp, tumor, or inflammation) in the upper airway and larynx

Outcomes

Primary Outcomes

Intubation time

Time Frame: Immediately after tracheal intubation completed

the time for tracheal intubation

Secondary Outcomes

  • Intubation-related complications(within 24 hours after surgery)
  • First-pass rate(Immediately after tracheal intubation completed)

Study Sites (1)

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