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临床试验/IRCT20221108056440N1
IRCT20221108056440N1招募中3 期

Comparison of the Effectiveness of l_arginine plus aspirin with aspirin alone in preventing adverse outcomes in pregnant women at high risk of preeclampsia

Kashan University of Medical Sciences0 个研究点目标入组 90 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
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
no limit 至 no limit(—)
性别
Female

入选标准

  • Pregnant women who are at high risk for preeclampsia
  • Pregnant women with a gestational age between 14 and 28 weeks of pregnancy
  • Previous history of pre-eclampsia in the individual or first degree relatives of the individual's sister or mother
  • Women with a history of chronic hypertension
  • Body mass index greater than 30
  • Multiple pregnancy
  • Lipid disorders

排除标准

  • Drug sensitivity to L-arginine
  • Drug sensitivity to aspirin

研究者

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