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This prospective randomized study aims to evaluate the effectiveness of intravenous lidocaine injection on the relief of pain in patients undergoing tonsillectomy.
A total of 62 patients will be randomized into one of two groups (group C or group I) based on Excel number generation.
Patients in group C will receive received normal saline intravenous injection, and patients in group I will receive an intravenous bolus injection of 1.5 mg/kg lidocaine followed by a continuous lidocaine infusion of 2 mg/kg/hr.
Visual analogue scale pain scores, fentanyl consumption and the frequency at which patients pushed the button (FPB) of a patient-controlled analgesia system will be recorded at 4, 12, 24, 48 hours postoperatively.
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62 participants in 2 patient groups, including a placebo group
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Central trial contact
Hyun Kang, Ph.D.
Data sourced from clinicaltrials.gov
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