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临床试验/IRCT20210511051268N1
IRCT20210511051268N1尚未招募3 期

The effect of premedication with oral acetaminophen on the prevention of localized pain from intravenous injection of propofol as induction agent in patients under general anesthesia

Tehran University of Medical Sciences0 个研究点目标入组 150 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
尚未招募
入组人数
150

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 years 至 60 years(—)
性别
All

入选标准

  • All patients for whom propofol is used as an induction of anesthesia

排除标准

  • Weight less than 50 kg
  • Chronic pain in any area of ??the body
  • High blood pressure
  • Cardiovascular disease
  • Cerebrovascular disease
  • Difficulty communicating (even if there is a marked drop in level of consciousness with the initial injection dose)
  • Abnormal liver function test results (AST and ALT more than twice normal)
  • Kidney failure or creatinine clearance greater than 1.2
  • Allergy to acetaminophen
  • Allergy to propofol
  • Patients in whom propofol is not used to induce anesthesia
  • Those who do not have a venous catheter in the back of the hand
  • Those whose catheter size is not 20G
  • those for whom we have to use rapid sequence induction for their anesthesia

研究者

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