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临床试验/IRCT201112198469N1
IRCT201112198469N1已完成未知

Clinical trial comparing the effect of 300 milligram intramuscular progesterone with oral nifedipine on threatened preterm labor in pregnant women hospitalized with threatened preterm labor

Iran University of Medical Sciences0 个研究点目标入组 80 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
80

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 45 years(—)
性别
Female

入选标准

  • Women aged 18-45 years; women with single pregnancy; women with pregnancy between 26-34 weeks of gestational age; women who referred with active uterine contractions and admitted for threatened preterm labor.
  • Exclusion criteria:
  • women with active labor phase (Cervical dilatation>3cm; vaginal bleeding; rapture of membrane; over distension of the uterus (multifetal gestation or polihydramnios); any systemic infection; oral temperature>38; intrauterine growth retard (IUGR) fetus; fetal distress; blood pressure>140/90 mmHg; any contraindication for progestrone or nifedipine administration; history of any thromboembolic disorders.

排除标准

  • 未提供

研究者

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