IRCT2017080117756N22已完成3 期
A clinical trial comparing administration versus non-administration of intravenous Dexamethasone on the incidence of headache after spinal anesthesia in women undergoing caesarean section
Vice-Chancellery for Research and Technology of Birjand University of Medical Sciences0 个研究点目标入组 104 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 104
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
- 15 years 至 45 years（—）
- 性别
- Female
入选标准
- •Age from 15 to 45 years; pregnant woman of Class 1 and 2 with uncomplicated term pregnancy according to the physical status classification by the American Society of Anesthesiologists; candidature for cesarean section surgery.
- •Exclusion criteria: Prohibition of spinal anesthesia (for example, coagulation disorders, peripheral neuropathy, infection of the needle insertion site, and spinal cord disorders); history of headache, migraine, and hypertension (as in eclampsia and preeclampsia).
排除标准
- 未提供
研究者
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