跳至主要内容
临床试验/NCT00133016
NCT00133016撤回不适用

The Efficacy of Early Amniotomy for Induction of Labor

University of Pennsylvania2 个研究点 分布在 1 个国家开始时间: 2006年8月最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
试验地点
2

研究概览

简要总结

The purpose of this clinical trial is to investigate the efficacy of early amniotomy on reducing both the duration of labor and the frequency of dystocia in nulliparous women undergoing an induction of labor. This research project is a prospective, parallel clinical trial, in which subjects are randomized into one of two treatment groups: those who undergo early amniotomy and those who do not undergo early artificial rupture of the amniotic membranes.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
盲法
None

入排标准

性别
Female
接受健康志愿者

入选标准

  • Gestational age > 37 weeks (using established National Institute of Child Health and Human Development [NICHD] dating criteria)
  • Nulliparous (i.e., first term pregnancy)
  • Admitted to the hospital for induction of labor
  • Singleton pregnancy
  • Fetal head applied to the cervix
  • The ability to understand the requirements of the study, as determined by the study nurse

排除标准

  • Premature rupture of amniotic membranes
  • Cervical dilation > 4 cm
  • Vaginal bleeding
  • Major fetal abnormalities that are known at time of admission

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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