TCTR20220419002已完成2 期
Furosemide for prevention 72 hours postpartum hypertension in women with preeclampsia with severe features: A randomized controlled trial
/A0 个研究点目标入组 80 人开始时间: 2022年4月19日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 80
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 N/A (No limit)（—）
- 性别
- Female
入选标准
- •Women who's 15 years old or more with preeclampsia with severe features who was undergone termination of pregnancy at 24 weeks' gestation or more
排除标准
- •1.pre-existing hypertension or taking antihypertensive medication
- •2.hypokalemia
- •3.history used of diuretic drug
- •4.unstable vital signs
- •5.allergy to furosemide or sulfonylurea
- •6.severe postpartum complication
研究者
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