NL-OMON39813已完成不适用
Hysmis Study Misoprostol for cervical priming prior to hysteroscopy in postmenopausal or nulliparous women; a multi-centre randomised placebo controlled trial - Hysmis Study
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 136
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 至 99（—）
入选标准
- •Indication for diagnostic or therapeutic hysteroscopy
- •Nulliparity if premenopausal
- •Postmenopausal state (>1 year after last menstruation)
- •Adequate command of the Dutch language
- •Informed consent
排除标准
- •Allergy for Misoprostol
- •Previous cervical surgery
- •Active infection
研究者
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Hysmis study.Misoprostol for cervical priming prior to hysteroscopy in postmenopausal or nulliparous women; a multi-centre randomised placebo controlled trial.Hysteroscopy/hysteroscopiePain/pijnMisoprostolNL-OMON22053VUmc136
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