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Curarisation and Intubation Conditions During Videolaryngoscopy With Glidescope Titanium — GICAC  

Tracheal Intubation Clinical Trial

Clinical Trial Summary

In this prospective, randomized study, the investigators assess the intubation conditions during videolaryngoscopy with Glidescope Titanium whether patients receive (curare (Atracurium) group) or no (control group) within elective surgery patients with no difficult intubation prediction

Clinical Trial Description

In this prospective, randomized study, the investigators assess the intubation conditions during videolaryngoscopy with Glidescope Titanium whether patients receive (curare (Atracurium)group) or no (control group) within elective surgery patients with no difficult intubation prediction. The IDS score assessed by an anesthesiologist from the video-recording is the primary outcome. All general anesthesias are standardized using Target Control Infusion of propofol and sufentanil. The investigators also compare IDS scores as assessed by intubators, time for tracheal intubation, and laryngeal morbidity in both groups. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02404142
Study type Interventional
Source CHU de Reims
Contact
Status Completed
Phase Phase 4
Start date February 20, 2015
Completion date August 5, 2016
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