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临床试验/IRCT20200127046280N1
IRCT20200127046280N1招募中2 期

The comparative evaluation of the effect of sublingual and cervical misoprostol on the duration of abortion in patients candidate for abortion in the first trimester of pregnancy

Qazvin University of Medical Sciences0 个研究点目标入组 200 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
入组人数
200

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
16 years 至 45 years(—)
性别
Female

入选标准

  • Unifetal pregnancy
  • Missed abortion
  • Fetal malformations
  • blighted ovum
  • Gestational age (12 weeks and less than 12 weeks )

排除标准

  • Rupture of membrane
  • History of cesarean section more than once
  • Multifetal pregnancy
  • History of allergy to misoprostol and prostaglandins
  • Contraindications of prostaglandin use ( like heart disease, kidney disease, history of seizures and hypotension )

研究者

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