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临床试验/IRCT2016072729103N1
IRCT2016072729103N1已完成未知

The effect of metoclopramide, propofol and dexamethasone in controlling nausea and vomiting during spinal anesthesia for cesarean section

Deputy of research and technology at azad university of Tehran0 个研究点目标入组 144 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
144

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 45 years(—)
性别
Female

入选标准

  • lack of hypertension in pregnancy; motion sickness; active bleeding; fetal distress; placental abruption; placenta Peravia; history of the gastrointestinal disease; systolic blood pressure less than 90 or hypotension more than 30% of the initial pressure.There is not any exclusive criteria.

排除标准

  • 未提供

研究者

发起方
Deputy of research and technology at azad university of Tehran

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