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临床试验/IRCT201404262080N15
IRCT201404262080N15已完成2 期

Comparison of transient neurologic symptoms induced by lidocaine and bupivacaine after spinal anesthesia in cesarean

Arak University of Medical Sciences, Vice Chancellor for Research0 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
2 期
状态
已完成
发起方
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
20 years 至 45 years(—)
性别
Female

入选标准

  • 1.Women between 20 to 45 years old
  • 2.Term pregnancy
  • 3.Elective cesarean
  • 4.No history of back pain, weakness and numbness in the extremities
  • Exclusion criteria:
  • 1.Underlying diseases such as pre-eclampsia and eclampsia Hypertension
  • 2.Adding epinephrine or opiate to drugs
  • 3.Using a needle with a larger size

排除标准

  • 未提供

研究者

发起方
Arak University of Medical Sciences, Vice Chancellor for Research

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