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临床试验/IRCT201204308588N6
IRCT201204308588N6已完成未知

Comparison of vaginal misoprostol with oral misoprostol in cervical priming before hystroscopic surgery in postmenopausal women and perimenopausal women without history of Normal Vaginal Delivery.

Tehran University of Medical Sciences.0 个研究点目标入组 120 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
已完成
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
40 years 至 no limit(—)
性别
Female

入选标准

  • menopausal women and perimenopausal women without history of normal vaginal delivery;who are not pregnant at the time of examination; do not have contraindications for prostaglandins(severe asthma, glaucoma, cardiac disease, hypertension or renal failure); do not have severe uterovaginal prolapse; do not have history of cervical surgery or cervical incompetency.Exclusion criteria: history of normal vaginal delivery in perimenopausal women;pregnancy; have contraindications for prostaglandins(severe asthma, glaucoma, cardiac disease, hypertension or renal failure); have severe uterovaginal prolapse;have history of cervical surgery or cervical incompetency.

排除标准

  • 未提供

研究者

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Effect of misoprostol in Cervical ripening | 临床试验