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临床试验/IRCT20100525004025N5
IRCT20100525004025N5已完成未知

Comparison of Misoprostol plus Isosorbide Mono Nitrate and Misoprostol plus placebo at the end of second trimester pregnancy.

Research deputy Kermanshah University of Medical Sciences0 个研究点目标入组 54 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
54

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

  • Gestational age 22-13 weeks can be a condition for entering the study.
  • nulliparous Can be a condition for entering the study.
  • Multiparous to parity 5 Can be a condition for entering the study.
  • singleton pregnancy can be a condition for entering the study.

排除标准

  • Women with contra indication of misoprostol (active Cardiac-pulmonary disease, Placenta Previa, history of 2 or more previous cesarean section, or history of major uterine surgeries such as myomectomy and uterine reconstruction surgery)Conditions for not admitting to study.
  • Women with contraindication of Isosorbide mono nitrate (IMN) (sensitivity to nitrates, hypotension, hypovolemia, heart disease, significant anemia Hb below 7 gr / dl and closed angle glaucoma )Conditions for not admitting to study.

研究者

发起方
Research deputy Kermanshah University of Medical Sciences

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