Clinical Trials Directory

Trials / Completed

CompletedNCT02404142

Curarisation and Intubation Conditions During Videolaryngoscopy With Glidescope Titanium

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
64 (actual)
Sponsor
CHU de Reims · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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

Detailed 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.

Conditions

Interventions

TypeNameDescription
DRUGCurare (Atracurium)Curare (Atracurium) versus saline isotonic solution for tracheal intubation
DRUGsaline isotonic solution

Timeline

Start date
2015-02-20
Primary completion
2016-04-05
Completion
2016-08-05
First posted
2015-03-31
Last updated
2018-01-09

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT02404142. Inclusion in this directory is not an endorsement.