Clinical Trials Directory

Trials / Completed

CompletedNCT02575716

Comparison of Intubating Condition of the Mcgrath Videolaryngoscope With and Without Muscle Relaxant

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
34 (actual)
Sponsor
Prince of Songkla University · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

The objective of this study was to evaluate intubating condition using the McGrath® VL Series 5, with and without muscle relaxant

Detailed description

Thirty-four patients with ASA classification I-II, who required oroendotracheal tube intubation, were studied in this prospective, double-blinded, randomized, clinical trial. Anesthesia was induced using fentanyl 1.5 mcg/kg, xylocaine 1.5 mg/kg and propofol 3 mg/kg. Patients were randomly assigned to one of the two groups to receive either rocuronium 0.6 mg/kg or saline intravenously. The Mcgrath® VL intubation was initiated after 90s, when the patients were fully relaxed. The primary outcome was to compare tracheal intubating conditions between two groups. The secondary outcomes were the success rate in the first attempt intubation, time to intubation, the required propofol dose for intubation and anesthetic complications. Statistical analyses were performed using the R program version 2.14.2. The level of statistical significance was set at p \< 0.05.

Conditions

Interventions

TypeNameDescription
DEVICEVideolaryngoscopeIntubation with McGrath video laryngoscope after muscle relaxant

Timeline

Start date
2013-03-01
Primary completion
2013-12-01
Completion
2014-03-01
First posted
2015-10-15
Last updated
2015-10-15

Locations

1 site across 1 country: Thailand

Source: ClinicalTrials.gov record NCT02575716. Inclusion in this directory is not an endorsement.