NCT01046708已完成不适用
Ovulation Induction With Clomiphene Citrate: to Support or Not to Support the Luteal Phase
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
- 300
- 主要终点
- ongoing pregnancy rate
研究概览
简要总结
The purpose of this study is to assess the effect of luteal phase supplement (LPS) on pregnancy rate in IUI cycles stimulated with clomiphene citrate.
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
- None
入排标准
- 年龄范围
- 18 Years 至 36 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Age ≤ 36 years
- •Body mass index between 18 and 29
- •Presence of both ovaries
- •Basal levels of estradiol (≤ 80 pg/ml) and progesterone (≤ 1.6ng/ml) on day one of the cycle and a day three FSH level of <12IU/L
- •Patients can enter the study only once.
- •Only the first IUI attempt will be included ( at the 2nd and 3 rd attempt progesterone could be administrated if it is necessary but these attempts will be excluded from the study)
- •Normal HSG (maximum 3 months prior starting the stimulation).
- •Donor sperm can be included
排除标准
- •Polycystic ovarian syndrome (Rotterdam criteria)
- •Endometriosis(≥AFS III)
研究组 & 干预措施
micronized progesterone
Experimental
干预措施: micronized progesterone (Drug)
结局指标
主要结局
ongoing pregnancy rate
时间窗: 1 year
次要结局
- implantation rate,clinical pregnancy rate(1 year)
研究者
Kyrou Dimitra
Doctor
Universitair Ziekenhuis Brussel
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