IRCT2014031717041N1已完成1 期
Efficacy of oral Furosemide in Postpartum Hypertension in Patients with Severe Preeclampsia in Kousar Hospital
Vice-Chancellor for research of Qazvin University of Medical Science0 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
- 1 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
- 15 years 至 45 years（—）
- 性别
- Female
入选标准
- •Inclusion criteria: All patients delivered of a pregnancy at or greater than 20 weeks of gestation and diagnosed with severe preeclampsia.
- •exclusion criteria: patients who had hypokalemia ( serum potassium less than 3 meq/l) on admission; patients who were already taking diuretics or potassium supplements for any reason; patients who demonstrated any hemodynamic instability surrounding the events of delivery.
排除标准
- 未提供
研究者
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