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Curarisation and Intubation Conditions During Videolaryngoscopy With Glidescope Titanium

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02404142
Acronym
GICAC
Enrollment
64
Registered
2015-03-31
Start date
2015-02-20
Completion date
2016-08-05
Last updated
2018-01-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tracheal Intubation

Keywords

Trachel intubation, IDS score, Videoaryngoscopy, Glidescope® Titanium®, NMBA, Curare (Atracurium)

Brief 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.

Interventions

DRUGCurare (Atracurium)

Curare (Atracurium) versus saline isotonic solution for tracheal intubation

Sponsors

Verathon
CollaboratorINDUSTRY
CHU de Reims
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Elective Surgery Adult Patients * no difficult intubation prediction

Design outcomes

Primary

MeasureTime frameDescription
IDS score video-assessed as described by Adnet et al. Measurement will be made by 2 experts anesthesiologists for centralized readingAssessment will be done at the end of the inclusions period (9 months)Number of IDS scores \<2 are compared

Secondary

MeasureTime frame
IDS score assesed by the intubator anesthesiologist3 days post intubation

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026