跳至主要内容
临床试验/IRCT2012103011324N1
IRCT2012103011324N1已完成2 期

Comparison between misoprostol and oxytocine in cervical ripening for labour induction: a randomized clinical trial

Ahwaz Jundishapur University of Medical Science, Vice Chancellor for Research and Technology0 个研究点目标入组 190 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
190

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

  • Entry criteria : Medical indication for the induction of delivery; Single twin pregnancies; Gestational age more than 36 weeks; Vertex presentation ;The normal heart rate of embryos .The exit criteria: The embryo-pelvic dystocia; An estimated weight of over 4000 grams or evidence of a lack of fitness cephalopelvic ; Abnormal vaginal bleeding or any placenta previa; The number of pregnancy over 4; Fetal malformation; Previous uterine scar; Any situation that does not cause vaginal delivery indication, Any contraindication use of misopristol ; Severe polyhydramnios

排除标准

  • 未提供

研究者

发起方
Ahwaz Jundishapur University of Medical Science, Vice Chancellor for Research and Technology

相似试验

Comparison between misoprostol and oxytocine in... | 临床试验