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

• Sponsor: University of Lausanne Hospitals (Other)
• Overall Status: Completed
• CT.gov ID: NCT02519647
• Collaborator: (none)
• Enrollment: 50
• Location: 1
• Arms: 2
• Actual Duration (Months): 10.1
• Patients Per Site Per Month: 5

Study Details

Study Description

Brief 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.

Condition or Disease	Intervention/Treatment	Phase
Nasal Obstruction; Lumbar Stenosis, Familial	Device: Tracheal intubation with Gliderite; Device: Tracheal intubation with S-guide	N/A

Detailed 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.

Study Design

• Study Type: Interventional
• Actual Enrollment: 50 participants
• Allocation: Randomized
• Intervention Model: Parallel Assignment
• Masking: Double (Participant, Outcomes Assessor)
• Primary Purpose: Supportive Care
• Official Title: Comparison of Intubation Conditions Between the Gliderite and the S-Guide in Patients With Simulated Difficult Airways
• Actual Study Start Date: Aug 1, 2015
• Actual Primary Completion Date: May 2, 2016
• Actual Study Completion Date: Jun 2, 2016

Arms and Interventions

Arm	Intervention/Treatment
Active Comparator: tracheal intubation with Gliderite Gliderite will be used for intubation	Device: Tracheal intubation with Gliderite; Tracheal intubation with Gliderite
Experimental: Tracheal intubation with S-Guide S-Guide will be used for intubation	Device: Tracheal intubation with S-guide; Tracheal intubation with S-guide

Outcome Measures

Primary Outcome Measures

1. Time necessary to intubate [50 seconds]

   Time needed to pass tracheal tube through vocal cords

Secondary Outcome Measures

1. Standardized questionnaire assessing injury after intubation [50 seconds]

   Assessment of discomfort after procedure

2. Standardized questionnaire assessing ease of use of the intubation [50 seconds]

   assessment by doctor of ease of intubation

3. Subjective ease of use of the intubation assessed by questionnaire [50 seconds]

   assessment by doctor of ease of intubation

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years and Older
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: Yes

Inclusion Criteria:

• Surgery necessitating general anesthesia and orotracheal intubation

Exclusion Criteria:

• History or criteria of difficult intubation

• Patient refusal

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Dpt of Anesthesiology, University of Lausanne CHUV	Lausanne	VD	Switzerland	1011

Sponsors and Collaborators

• University of Lausanne Hospitals

Investigators

• Principal Investigator: patrick Schoettker, MD, PD, University of Lausanne Hospitals

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

• commercial description of S-Guide provider

Publications

None provided.

• Responsible Party: Patrick Schoettker,MD PD, MD, PD, University of Lausanne Hospitals
• ClinicalTrials.gov Identifier: NCT02519647
• Other Study ID Numbers: 267/15
• First Posted: Aug 11, 2015
• Last Update Posted: Mar 2, 2020
• Last Verified: Feb 1, 2020

• Additional relevant MeSH terms: Nasal Obstruction

Study Results

No Results Posted as of Mar 2, 2020