Comparison of Intubation Conditions Between the Gliderite and the S-Guide

Nasal Obstruction Clinical Trial

— S-Guide  

Official title:

Comparison of Intubation Conditions Between the Gliderite and the S-Guide in Patients With Simulated Difficult Airways

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02519647
• Other study ID #: 267/15
• Status: Completed
• Phase: N/A
• Start date: August 1, 2015
• Est. completion date: June 2, 2016

Study information

• Verified date: February 2020
• Source: University of Lausanne Hospitals
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Intubation with an unchanneled videolaryngoscope mandates the use of a stylet. The Gliderite is a stylet specially designed for videolaryngoscopes. The investigators aim to compare the efficacy of a new designed bougie for intubation in patients with simulated difficult airways.

Description:

Intubation with an unchanneled videolaryngoscope mandates the use of a stylet. The Gliderite is a stylet specially designed for videolaryngoscopes. The investigators aim to compare the efficacy of a new designed bougie for intubation in patients with simulated difficult airways.

The primary endpoint will be time necessary for intubation, secondary endpoints will be injuries, ease of use and subjective assessment.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 50
• Est. completion date: June 2, 2016
• Est. primary completion date: May 2, 2016
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Surgery necessitating general anesthesia and orotracheal intubation

Exclusion Criteria:

• History or criteria of difficult intubation

• Patient refusal

Related Conditions & MeSH terms

• Lumbar Stenosis, Familial
• Nasal Obstruction

Intervention

Device:
• Tracheal intubation with Gliderite
Tracheal intubation with Gliderite
• Tracheal intubation with S-guide
Tracheal intubation with S-guide

Locations

Country	Name	City	State
Switzerland	Dpt of Anesthesiology, University of Lausanne CHUV	Lausanne	VD

Sponsors (1)

Lead Sponsor	Collaborator
University of Lausanne Hospitals

Country where clinical trial is conducted

Switzerland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Time necessary to intubate	Time needed to pass tracheal tube through vocal cords	50 seconds
Secondary	Standardized questionnaire assessing injury after intubation	Assessment of discomfort after procedure	50 seconds
Secondary	Standardized questionnaire assessing ease of use of the intubation	assessment by doctor of ease of intubation	50 seconds
Secondary	Subjective ease of use of the intubation assessed by questionnaire	assessment by doctor of ease of intubation	50 seconds

External Links

•   commercial description of S-Guide provider