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
| Type | Name | Description |
|---|---|---|
| DRUG | Curare (Atracurium) | Curare (Atracurium) versus saline isotonic solution for tracheal intubation |
| DRUG | saline 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.