NCT01156948Unknown3 期
Comparison of Vaginal Versus Oral Misoprostol for Nulliparous Women Prior to Operative Hysteroscopy
适应症
干预措施
相关药物
试验速览
- 阶段
- 3 期
- 入组人数
- 120
- 试验地点
- 1
- 主要终点
- cervical width
研究概览
简要总结
To compare the impact of 400-microgram self-administered vaginal versus self-administered oral misoprostol at home on preoperative cervical ripening in nulliparous women prior to outpatient hysteroscopy.
详细描述
There is no consensus on the effect of misoprostol on cervical ripening for nulliparous women. The aim of the study is to compare the impact of 400-microgram self-administered vaginal versus self-administered oral misoprostol at home on preoperative cervical ripening in nulliparous women prior to outpatient hysteroscopy.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double (Participant, Investigator)
入排标准
- 年龄范围
- 16 Years 至 40 Years（Child, Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •nulliparous women who are referred to outpatient hysteroscopy and who have given informed consent will be eligible for study recruitment.
排除标准
- •women with a known allergy to misoprostol.
研究组 & 干预措施
vaginal misoprostol
Active Comparator
vaginal misoprostol was administered to this group of nulliparous women
干预措施: misoprostol (Drug)
oral misoprostol
Experimental
oral misoprostol
干预措施: oral misoprostol (Drug)
结局指标
主要结局
cervical width
时间窗: one day
次要结局
- side effects(one day)
研究者
研究点 (1)
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