跳至主要内容
临床试验/NL-OMON22488
NL-OMON22488招募中不适用

Potential effect of proton-pump inhibitor on angiogenic markers in preeclampsia

one0 个研究点目标入组 44 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
one
入组人数
44

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

入选标准

  • Women (=18 years) with a singleton pregnancy diagnosed with PE with a gestational age of = 20 weeks and <35 weeks admitted to the obstetric department who give written informed consent, will be included.

排除标准

  • - Multiple pregnancies
  • - Not willing to give written informed consent.
  • - Other reasons than (suspected) PE requiring hospitalization
  • - The use of PPI at time of randomization
  • - Contraindications or hypersensitivity to PPI use
  • - The use of medication affected by PPI
  • - Fetal death at time of inclusion
  • - Signs of fetal distress at time of inclusion
  • - Expected delivery of = 2 days

研究者

发起方
one

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