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临床试验/IRCT20191123045476N2
IRCT20191123045476N2招募中3 期

Evaluation of the efficacy of dilapane-S gel in comparison with misoprostol during pre-hysteroscopic cervical preparation

Iran University of Medical Sciences0 个研究点目标入组 120 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
招募中
入组人数
120

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
49 years 至 52 years(—)
性别
Female

入选标准

  • Postmenopausal women (at least 1 year after the last menstrual cycle) or Nolipar or Multipar who have no history of natural childbirth are candidates for hysteroscopic surgery due to uterine myoma and uterine polyp.
  • Postmenopausal women (at least more than 1 year after the last menstrual cycle) or Nolie Par or Multipar who have no history of normal delivery are candidates for hysteroscopic surgery due to increased endometrial thickness confirmed by ultrasound or abnormal vaginal bleeding

排除标准

  • Contraindications to hysteroscopy
  • Recent or current pelvic infections
  • Previous cervical surgery
  • Confirmed cervical or breast malignancies
  • Vaginal delivery history
  • Hypersensitivity to misoprostol and prostaglandins

研究者

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