PACTR201604001597634尚未招募未知
The effect of goal directed fluid, inotrope and vasopressor therapy in preeclamptic patients undergoing caesarean section delivery under spinal anaesthesia with the use of a non-invasive finger cuff cardiac output monitor
Department of Anaesthesiology0 个研究点目标入组 60 人开始时间: 2016年4月21日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 发起方
- 入组人数
- 60
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 Year(s) 至 45 Year(s)（—）
- 性别
- Female
入选标准
- •Pregnant patients, 18 years of age and older, with the diagnosis of preeclampsia (as per the attending obstetrician), undergoing caesarean section delivery under spinal anaesthesia will be included in the study.
排除标准
- •-with fetal distress
- •-unable to give informed consent (including failure to understand explanation of the study in English language)
- •-who decline to participate
- •-already on vasopressor therapy prior to arrival in theatre
- •-with antepartum haemorrhage
- •-expected to have general anaesthesia
- •-converted from spinal to general anaesthesia intraoperatively
- •-where there is deviation from the study protocol
研究者
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