NCT01354834已完成不适用
Assessment of the Clinical Efficacy of Menopur® in Intrauterine Artificial Insemination (From Partner or From Donor)
适应症
干预措施
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 207
- 试验地点
- 1
- 主要终点
- Clinical pregnancy rate
研究概览
简要总结
The purpose of this study is to assess the effectiveness of Menopur to achieve clinical pregnancy in females undergoing intrauterine insemination in clinical practice.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 40 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Infertile couples for over one year (primary or secondary) or infertile women (or not) with indication of PAI or DAI
- •Seminal sample suitable for artificial insemination treatment according to the criterion of each centre
- •Patient prescribed therapy with Menopur in artificial insemination
排除标准
- •Contraindications to intrauterine insemination
- •Contraindications to Menopur
研究组 & 干预措施
hMG
干预措施: hMG (Drug)
结局指标
主要结局
Clinical pregnancy rate
时间窗: 30 days
次要结局
- Live birth rate(40 weeks)
研究者
研究点 (1)
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