跳至主要内容
临床试验/IRCT20181115041666N1
IRCT20181115041666N1尚未招募早期 1 期

Investigation of maternal and neonatal outcomes of expectant treatment in pregnant women with preterm premature rupture of membranes (PPROM) in hospital compared with expectant treatment at home

Mashhad University of Medical Sciences0 个研究点目标入组 100 人开始时间: 待定最近更新:
适应症

试验速览

阶段
早期 1 期
状态
尚未招募
入组人数
100

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

  • alive singleton pregnancy
  • Gestational age between 25 and 34 weeks
  • The absence of chorioamnionitis symptoms
  • The lack of evidence for fetal distress
  • No vaginal bleeding
  • Patient's consent
  • Evaluation for 72 hours in hospital
  • Cephalic presentation
  • Having a caretaker at home
  • Taking 60 minutes at most to reach the first treatment center
  • The diameter of maximum vertical pocket of the amniotic fluid is more than 2 Cm²

排除标准

  • Occurrence of chorioamnionitis
  • disturbed fetal tests of health evaluation
  • Vaginal bleeding
  • Patient's unwillingness to continue participation in the study
  • Gestational age of less than 25 weeks of labor (greater than 3 cm of dilatation)

研究者

相似试验