The goal of this clinical trial is to compare Efficacy of low dose propofol(0.5 mg/kg) vs placebo given at the end of sevoflurane anesthesia for prevention of emergence agitation in pediatric patient undergoing MRI scan. The main question it aims to answer is "Can low dose propofol reduce the incidence of emergence agitation after general anesthesia?" Participants will be given propofol 0.5 mg/kg or saline according to the allocated group at the completion of MRI scan
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
TRIPLE
Enrollment
134
recieve propofol 0.5 mg/kg intravenously at end of sevoflurane anesthesia
recieve propofol 0.5 mg/kg intravenously at end of sevoflurane anesthesia
Khon kaen University
Khon Kaen, Muang, Thailand
incidence of emergence agitation
Time frame: at 5,10,15,20,25,30 minutes after extubation
Incidence of complication
Nausea or vomiting, airway obstruction, laryngospasm, desaturation and apnea
Time frame: 2 hours after extubation
Use of rescue medication
use of ondansetron, atropine
Time frame: 2 hours after extubation
Emergence time
duration of emergence
Time frame: 2 hours after extubation
Length of stay in post anesthetic care unit
Time frame: 2 hours after extubation
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