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临床试验/IRCT2016022426745N1
IRCT2016022426745N1已完成未知

Comparison the effects of the isosorbide mononitrate with misoprostol and misoprostol with placebo for cervical ripening in induction of labour in 41 week pregnancies.

Vice Chancellor for Research, Mashhad university of medical sciences0 个研究点目标入组 186 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
186

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

  • The inclusion criteria are first pregnancies aged more than 41 weeks based on the sonography; with single; normal fetus; and cephalic presentation with no complication and before induction bishop score less than 6.
  • Exclusion criteria include known allergy for prostaglandins or mifepristone; any contraindication for induction (such as uterine scar); contraindications for mifepristone administration (like adrenal, renal or liver disease); major cephalopelvic disproportion; abnormal stress test; vaginal bleeding and sever oligohydramnios.

排除标准

  • 未提供

研究者

发起方
Vice Chancellor for Research, Mashhad university of medical sciences

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