跳至主要内容
临床试验/IRCT201702282624N22
IRCT201702282624N22已完成2 期

A comparison between induction of labor with 3 methods of titrated oral misoprostol, constant dose of oral misoprostol and folly catheter with extra amniotic saline infusion (EASI), in women with unfavorable cervix.

Vice chancellor for research ,Iran University of Medical Sciences.0 个研究点目标入组 116 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
116

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
18 years 至 40 years(—)
性别
Female

入选标准

  • Inclusion criteria : maternal age between 18-40 years old; gestational age of more than 37 weeks ; singleton, cephalic presentation, intact membrane and Bishop Score of less than 6. Exclusion criteria : any sign of fetal distress; placenta previa and any vaginal bleeding of more than bloody show; history of any surgery on uterus including cesarean section; known uterine anomaly; intra uterine fetal death, and known hypersensitivity to misoprostol.

排除标准

  • 未提供

研究者

发起方
Vice chancellor for research ,Iran University of Medical Sciences.

相似试验