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临床试验/IRCT20181107041585N4
IRCT20181107041585N4已完成2 期

Comparing the efficacy of 17a hydroxyprogesterone caproate ( proluton) versus vaginal progesterone (cyclogest) on perinatal outcome in high risk patients who undergo cerclage

Vice chancellor for research, Hormozgan University of Medical Sciences0 个研究点目标入组 58 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
58

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

  • History of more than two previous preterm birth less than 34 weeks
  • Singleton pregnancy
  • Cervical length less than 25 mm based on latest vaginal sonography

排除标准

  • Fetal anomaly
  • Uterine cramp at the time of study
  • Vaginal bleeding at the time of study
  • Preterm rupture of membrane
  • Allergy to hormonal therapy

研究者

发起方
Vice chancellor for research, Hormozgan University of Medical Sciences

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