Video Laryngoscope, New Intubation Device

Phase 2

Completed

• Conditions: Elective Intubation

• Registration Number: NCT02095470
• Lead Sponsor: Shiraz University of Medical Sciences

Brief Summary

new glidoscope was tested on 401 patients

Detailed Description

Four hundred and one patients who were scheduled for elective operation, were randomly assigned to be intubated by direct laryngoscopy using a Macintosh blade size 3rd (DL, n=196) or intubation using the video laryngoscope (VL, n=205). Prior to intubation all patients were given a similar regimen of induction of anesthesia. The patients were then intubated, using direct laryngoscopy or the VL, by a different anesthetist during which the larynx was inspected and given a laryngoscopy score. Time to intubate, failure rate, injuries, personnel pleasure and, aspiration rate were measured

Study Timeline

• Study Start: 2013-02
• Primary Completion: 2014-01
• Study Completion: 2014-02
• Status Verified: 2014-03
• Study First Submitted: 2014-03-15
• Study First Submitted QC: 2014-03-20
• Last Update Submitted: 2014-03-20
• Study First Posted: 2014-03-24
• Last Update Posted: 2014-03-24

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 401

Inclusion Criteria

• elective operation who filled the consent

Exclusion Criteria

• poor intubation
• emergency cases
• hemodynamic derangement

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
unsuccessful attempts	60 minutes	number of failure
laryngoscopy grade	hospital stay (average 48 hours)	grade of laryngoscopy
time to intubation	60 minutes	time to successful intubation in minutes

Secondary Outcome Measures

Name	Time	Method
aspiration	hospital stay ( 48 hours)	clinical aspiration or radiological

Trial Locations

Locations (1)

Shiraz Universty of Mesical Sciences; 🇮🇷 Shiraz, Fars, Iran, Islamic Republic of