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临床试验/IRCT2013062213737N1
IRCT2013062213737N1已完成未知

The effect of chamomile capsule on obstetrical outcomes in post term pregnancy

Tehran University of Medical Sciences0 个研究点目标入组 70 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
70

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

  • Inclusion criterias: pregnant women 18-35 years old; Iranian nationality; have a body mass index less than 30 before pregnancy; low risk pregnancy; with getational age 41 weeks (40 weeks completely) based on LMP or ultrasound in first trimester; no history of recurrent abortion; infertility and undesirable outcomes of pregnancy; single pregnancy; cephalic presentation; alive fetus; weight of fetus between 2500-4000 gram based on physical examination or ultrasonography; cervical bishop score less than 4; intact membranous; normal pelvic according to researcher's exam; normall fetal heart rate and BPP and NST; no sensivity to herbal drugs and non-addicted persons.
  • Exclusion criterias: those who consume them is less than one capsule per day, more than one care session is absent, and appears allergic symptoms.

排除标准

  • 未提供

研究者

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