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临床试验/IRCT2017041527677N7
IRCT2017041527677N7已完成2 期

Comparison the effect of intravenous ondansetron and sub-hypnotic propofol dose on pruritus after intrathecal opioid in patient with elective cesarean surgery

Vice Chancellor for research of Urmia 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
2 期
状态
已完成
发起方
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 40 years(—)
性别
Female

入选标准

  • 20 to 40 years old; patient with class I and II America society of Anesthesiologists; cesarean surgery with spinal anesthesia
  • Exclusion criteria: any complaints of pruritus before surgery; start pruritus before closing cord; allergy to medications; preeclampsia; eclampsia; people who had used anti-nausea drug in the past 24 hours.

排除标准

  • 未提供

研究者

发起方
Vice Chancellor for research of Urmia University of Medical Sciences

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