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临床试验/IRCT201408114365N17
IRCT201408114365N17已完成2 期

Effect of intravenous Lidocaine on pain intensity after Cesarean section

Vice chancellor for research of Mazandaran University of Medical Sciences0 个研究点目标入组 100 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
100

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 35 years(—)
性别
Female

入选标准

  • willingness to enter the study and informed written consent; ASA class 1&2; Elective cesarean surgery; Age between 20 and 35 years.
  • Exclusion criteria: Unwillingness to continue the study; Known lidocaine sensitivity; surgery time more than 1/5 hours; Midline incision for any reason; Any unusual complication during surgery.

排除标准

  • 未提供

研究者

发起方
Vice chancellor for research of Mazandaran University of Medical Sciences

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