跳至主要内容
临床试验/KCT0002246
KCT0002246已完成未知

The effect of intravenous dexmedetomidine versus propofol for postoperative analgesia in ankle surgery with spinal anesthesia

Samsung Medical Center0 个研究点目标入组 44 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
入组人数
44

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional Study

入排标准

年龄范围
20(Year) 至 69(Year)(—)
性别
All

入选标准

  • Patients who performed a Arthroscopic debridement & Brostrom operation under spinal anesthesia( 20 years or more, under 70 years)
  • ASA physical status I,II,III

排除标准

  • Patients who refuse spinal anesthesia
  • Pateints who used opioids over a long period of time(30 mg/d of oral morphine or the equivalent) or had a serious side effect of opioid.
  • Pateints who have a history of serious side effect of dexmedetomidine or propofol
  • Patients who have significant coagulopathy or generalized infection
  • Patients with history of heart disease, liver or kidney dysfuncion
  • Patients who is unable to voluntarily agree to participate in the research

研究者

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