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
| Type | Name | Description |
|---|---|---|
| DEVICE | Videolaryngoscope | Intubation 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.