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临床试验/IRCT20200217046523N14
IRCT20200217046523N14招募中2 期

Comparative study of the effect of vaginal consumption of primrose oil with vaginal misoprostol on cervical preparation in nulliparous women with prolonged pregnancy

Esfahan University of Medical Sciences0 个研究点目标入组 110 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
招募中
入组人数
110

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 35 years(—)
性别
Female

入选标准

  • Duration of pregnancy 40 weeks and more
  • Primiparous women
  • Single delivery
  • Satisfaction to participate in the study
  • Age between 18- 35 years

排除标准

  • The patient refuses to continue attending the study for various reasons
  • Patient discharge with personal consent

研究者

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