跳至主要内容
临床试验/IRCT20141209020258N158
IRCT20141209020258N158招募中3 期

Comparison of onset, duration and quality of supraclavicular block using 0.5% bupivacaine with magnesium sulphate , ketamine and neostigmine in forearm orthopedic surgery

Arak University of Medical Sciences0 个研究点目标入组 90 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
招募中
入组人数
90

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
20 years 至 70 years(—)
性别
All

入选标准

  • 20 -70 years
  • Candidate for upper limb orthopedic surgery
  • No more than one fracture in the body or surgery
  • No blood coagulation diseases and disorders in PTT, PT and INR
  • Body mass index less than 35
  • Lack of psychological problems
  • No pregnant
  • Absence of neurological disorders in the hand
  • No allergies to drugs used
  • Absence of chronic pain syndrome

排除标准

  • Lack of patient cooperation to perform the block
  • Block failure
  • Surgery time less than 50 and more than 150 minutes
  • Need for more sedation than stated in the plan

研究者

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