跳至主要内容
临床试验/IRCT20210114050036N1
IRCT20210114050036N1已完成3 期

Comparison of two different doses of intrathecal ropivacaine on onset and duration of sensory and motor block in patients undergoing cesarean section with spinal anesthesia

Yazd University of Medical Sciences0 个研究点目标入组 66 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
66

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
18 years 至 40 years(—)
性别
Female

入选标准

  • Term pregnancy
  • ASA Class 1
  • Candidates for non-emergency cesarean section under the spinal anesthesia

排除标准

  • Fetal anomalies
  • Heart, liver, kidney or cerebrovascular diseases
  • Preeclampsia and eclampsia
  • Weighting less than 50 kg or more than 100 kg
  • Sensitivity to any of the drugs used in the study
  • For any reason that the patient needs general anesthesia
  • Patient dissatisfaction for entering to the study

研究者

发起方
Yazd University of Medical Sciences

相似试验