NCT00708539Unknown4 期
A Prospective Randomized Multicentre Study to Compare Crinone 8% Once Daily Versus Other Vaginal Progesterone.
Nordica Fertility Clinic17 个研究点 分布在 2 个国家目标入组 2,686 人开始时间: 2006年4月最近更新:
适应症
干预措施
相关药物
试验速览
- 阶段
- 4 期
- 发起方
- 入组人数
- 2,686
- 试验地点
- 17
- 主要终点
- Equivalence in ongoing pregnancy per embryo transfer between the two groups
研究概览
简要总结
To compare the effect of Crinone 8% administered once daily versus other vaginal progesterone in terms of ongoing pregnancy rate 5 weeks after embryo transfer as well as patient convenience.
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
- Single (Outcomes Assessor)
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
- •18-40 years
- •Regular menstrual cyclus 25-35 days
- •both ovaries present
- •No more than 2 previous IVF attempts
- •Have given written informed consent
排除标准
- •More than 2 previous attempts
- •Known drug abuse
- •Known allergies to the study medication
- •No embryo transfer performed in the study cycle
- •Previous participating in the study
研究组 & 干预措施
1
Active Comparator
Crinone vaginal gel 8% 90 mg once daily
干预措施: Progesterone (Drug)
2
Active Comparator
Progesterone mic 400 mg three times daily
干预措施: Progesterone (Drug)
结局指标
主要结局
Equivalence in ongoing pregnancy per embryo transfer between the two groups
时间窗: week 5 after embryo tranfer
次要结局
- Convenience for the patient(the treatment period (from the day of embryo transfer and 19 days ahead))
研究者
研究点 (17)
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