The objective of this study was to evaluate intubating condition using the McGrath® VL Series 5, with and without muscle relaxant
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.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
34
Intubation with McGrath video laryngoscope after muscle relaxant
Department of anesthesiology
Hat Yai, Changwat Songkhla, Thailand
Intubating condition.
number of participants with 34 people
Time frame: one year
Success rate in the first attempt intubation.
Time frame: one year
Time to intubation
Time frame: One year
The required propofol dose for intubation without muscle relaxant.
Time frame: one year
Events during the intubation attempts occurred.
Time frame: one year
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