NCT01816802Unknown不适用
MERGE: MulticEnter ReGistry With Eeva
适应症
试验速览
- 阶段
- 不适用
- 入组人数
- 1,200
- 试验地点
- 12
- 主要终点
- Clinical Pregnancy Rate
研究概览
简要总结
The purpose of this study is to record and evaluate the use of traditional morphology grading combined with Eeva in the treatment of in vitro fertilization.
详细描述
This is a prospective, observational, single-arm, nonrandomized, multicenter study. Data will be collected to establish eligibility, at baseline, during the stimulation and in vitro fertilization process, during embryo culture, at embryo transfer, at 12-18 days post egg retrieval to verify biochemical pregnancy, and then typically at 5-6 weeks gestational weeks to verify clinical pregnancy.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •women undergoing fresh in vitro fertilization treatment using their own eggs or donor eggs.
排除标准
- •history of cancer.
- •gestational carrier.
结局指标
主要结局
Clinical Pregnancy Rate
时间窗: 5-6 gestational weeks
Determined by first pregnancy ultrasound outcome and optional 12-month phone follow-up
次要结局
未报告次要终点
研究者
研究点 (12)
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