跳至主要内容
临床试验/NL-OMON50177
NL-OMON50177招募中4 期

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

Erasmus MC, Universitair Medisch Centrum Rotterdam0 个研究点目标入组 44 人开始时间: 待定最近更新:
适应症

试验速览

阶段
4 期
状态
招募中
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

年龄范围
18 至 99(—)

入选标准

  • Women (>=18 years) with a singleton pregnancy diagnosed with PE with a
  • gestational age between >= 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

相似试验