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临床试验/IRCT20230722058884N1
IRCT20230722058884N1招募中3 期

Assessing the clinical effects of a short-term course of Oral Furosemide in postpartum period in patients with preeclampsia during pregnancy : A Randomized Controlled Trial

Iran University of Medical Sciences0 个研究点目标入组 118 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
招募中
入组人数
118

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 no limit(—)
性别
Female

入选标准

  • All patients who have had a recent pregnancy with preeclampsia

排除标准

  • Age under 18
  • Patients with prior history of hypertension
  • Patients with renal disease
  • Patients with history of congenital heart defects

研究者

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