跳至主要内容
临床试验/KCT0002933
KCT0002933进行中(未招募)未知

Determination of the minimum effective concentration (MEC90) of dexmedetomidine for prolonged analgesia in patients undergoing interscalene brachial plexus block

Samsung Medical Center0 个研究点目标入组 60 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
进行中(未招募)
入组人数
60

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

  • Adult (>20 years old or =20, <70 years old)
  • patients with written informed consent
  • American society of anesthesiologist physical status I-III: Previous healthy (I), controlled systemic disease (II), uncontrolled systemic disease (III)

排除标准

  • American society of anesthesiologist physical status higher than IV
  • Child or old age
  • Sensory or motor deficit
  • Allergy to local anesthetic
  • Allergy to dexmedetomidine
  • Local infection at the site of interscalene brachial plexus block or systemic infection
  • Hepatic, cardiac, or renal disease
  • Coagulopathy (Prolonged INR>1.5)
  • Patient refusal

研究者

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