跳至主要内容
临床试验/NCT03025503
NCT03025503Unknown不适用

Nipple Stimulation for Labor Induction: Efficiency, Safety and Satisfaction Measures

Hadassah Medical Organization1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2017年1月最近更新:
适应症

试验速览

阶段
不适用
入组人数
100
试验地点
1
主要终点
progression to active labor as measured by the Bishop score

研究概览

简要总结

This study will examine the use of nipple stimulation for cervical ripening in women who present to the labor and delivery ward after their water has broken but have a contraindication to prostaglandins.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Week 37 + 0 and on
  • PROM (premature rupture of membranes)
  • Multiparity (birth sixth or higher) or TOLAC (trial of labor after Caesarean section)
  • Not in active labor - without regular contractions fetal monitor, cervical dilation < 4 cm and effacement < 80%.

排除标准

  • Water break > 24 hours at the time of admission to the delivery room
  • Active vaginal bleeding with suspected placental abruption
  • Maternal fever
  • Multifetal pregnancy
  • Women with contraindication for vaginal birth
  • Preeclampsia
  • IUGR (intrauterine growth restriction)
  • Macrosomia
  • Non-reassuring fetal heart tracing

结局指标

主要结局

progression to active labor as measured by the Bishop score

时间窗: 6 hours

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验