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临床试验/IRCT138903121096N3
IRCT138903121096N3已完成2 期

Comparison of Sublingual and vaginal Misoprostol for labor induction in primiparous women

Vice chancellor for research -Guilan university of medical sciences0 个研究点目标入组 126 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
126

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
15 years 至 45 years(—)
性别
Female

入选标准

  • a) single pregnancy (between 36 to 42 weeks), b) vertex presentation, c) intact fetal membrane, d) bishop score equal or less than four e) absence of uterus spontaneous contractions f) fetal weight less than 4000gr j) normal fetal heart rate h) cephalopelvic proportion Exclusion criteria: a) sensitivity to PGs b) previous history of cesarean c) uterus wall scar d) preeclampsia or blood pressure more than 140/90 mmhg e) PROM f) vaginal bleeding

排除标准

  • 未提供

研究者

发起方
Vice chancellor for research -Guilan university of medical sciences

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