Pain Clinical Trial
Official title:
Systemic Magnesium to Improve Postoperative Pain in Pediatric Patients Undergoing Tonsillectomy: A Randomized, Double Blinded, Placebo Controlled Trial
This study is a double-blind randomized controlled trial using intravenous magnesium versus
placebo to determine if systemic magnesium can decrease postoperative pain in pediatric
patients undergoing tonsillectomy.
Participants will be in one of two arms. Those in Arm 1 will receive magnesium (30 mg/kg
bolus followed by a 10mg/kg/hr infusion) while those in Arm 2 will receive an equal volume of
normal saline bolus followed by infusion (placebo).
The primary objective is to determine if systemic magnesium will decrease postoperative pain
in patients undergoing tonsillectomy. The secondary objectives will determine if systemic
magnesium administration is associated with a decrease in opioid-related side effects,
decrease the incidence of emergence delirium, and improve postoperative functional recovery.
The study hypothesis is that the use of intravenous magnesium will decrease postoperative
pain, decrease opioid-related side effects, decrease the incidence of emergence delirium, and
improve functional recovery in patients undergoing tonsillectomy.
n/a
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