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临床试验/IRCT20230522058253N1
IRCT20230522058253N1尚未招募3 期

Comparison of frequency of Natural vaginal delivery after preparation of cervix with evening primrose, EASI mechanical method and misoprostol in 41 week pregnant women

Hamedan University of Medical Sciences0 个研究点目标入组 420 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
尚未招募
入组人数
420

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

  • Primiparous women at 41 weeks are candidates for termination of pregnancy by natural delivery method

排除标准

  • Pregnant women with IUFD, SGA, IUGR
  • Pregnant women with spotting and abnormal placenta

研究者

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