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临床试验/IRCT2015040721506N2
IRCT2015040721506N2已完成1 期

Comparison extra amniotic salin infusion and vaginal isoniazide for cervical ripening before induction and labour duration in term and post term pregnancy

Iran University of Medical Sciences0 个研究点目标入组 150 人开始时间: 待定最近更新:

试验速览

阶段
1 期
状态
已完成
入组人数
150

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
17 years 至 43 years(—)
性别
Female

入选标准

  • 1- single tone pregnancy 2- bishop score<5.
  • Exclusion criteria: 1-macrosomia EFW> 5 Kg. 2- not reassuring NST. 3- PROM 4-AFI<5 Cm. 5- history of kidney and liver diseases. 6-history of Cesarian section. 7- low lying placenta. 8- any contraindication of isoniazide such as vomiting, nausea, visual defect, vertigo. 9- no cephalic presentation. 10- unexplained vaginal bleeding. 11- labor phase. 12- organic disease. 12- grand multiparity

排除标准

  • 未提供

研究者

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