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临床试验/IRCT201603243860N24
IRCT201603243860N24已完成2 期

Evaluation of Saffron capsule on cervical ripening, beginning and delivery outcomes in primiparous women

Vice Chancellor for research of Shahid Beheshti University of Medical Sciences0 个研究点目标入组 100 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
100

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 35 years(—)
性别
Female

入选标准

  • primiparous woman; age between 18 to 35 years; gestational age of 40 weeks or more; singleton pregnancy with cephalic presentation; not starting uterine contraction; Bishop score less than or equal 4; intact amniotic sac; normal pattern of fetal heart rate; reactive non-stress test; fetal weight between 2500 to 4000; low-risk pregnancy (without known surgical diseases and internal disease or pregnancy complications such as preeclampsia, placental abruption, previa and the absence of known fetal problems); avoiding the use of herbal medicines, chemical or traditional methods for induction of labor in 36 hours before treatment; lack of sex from 24 hours before the beginning till end of the study.
  • Exclusion criteria: Use of oral Saffron; cephalo-pelvic disproportion; using uterine stimulant drugs during the study, such as castor oil; obstetric emergency cases.

排除标准

  • 未提供

研究者

发起方
Vice Chancellor for research of Shahid Beheshti University of Medical Sciences

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