EUCTR2011-005160-23-NL进行中（未招募）不适用
Hismys study. Misoprostol for cervical priming prior to hysteroscopy in postmenopausal and nulliparous premenopausal women; a multi-centre randomised placebo controlled trial - Hysmis
VU medical center0 个研究点开始时间: 2013年4月11日最近更新:
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- Female
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
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 68
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 68
排除标准
- •Allergy for misoprostol
- •Previous cervical surgery or hysteroscopy
- •Active infection
研究者
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