EUCTR2012-001622-10-CZ进行中（未招募）不适用
A randomised, placebo-controlled, double-blind, parallel groups, multinational, multicentre trial assessing the effect of barusiban administered subcutaneously on the day of transfer on implantation and pregnancy rates in IVF/ICSI patients - BASIC
适应症
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 入组人数
- 340
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- Female
入选标准
- •- Women aged 18-37 years
- •- Women who have undergone 2-4 previous fresh IVF/ICSI cycles that all resulted in a negative ßhCG test, despite transfer of at least one embryo/blastocyst of good quality
- •- Women who have in the current controlled ovarian stimulation cycle for IVF/ICSI followed the long GnRH agonist or GnRH antagonist protocol, received hCG for triggering of final follicular maturation and have undergone oocyte retrieval for IVF/ICSI with the purpose of fresh transfer
- •- Retrieval of at least 6 oocytes in the current controlled ovarian stimulation cycle
- •- Subjects should have at least one embryo of good quality available for transfer on day 3, or one expanded or hatching/hatched blastocyst available for transfer on day 5
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 340
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •- A total of 6 or more controlled ovarian stimulation cycles for IVF/ICSI
- •- Abnormal karyotype
- •- Uterine pathology or hydrosalpinx
- •- Diagnosed with acquired or congenital thrombophilia disease
研究者
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