EUCTR2012-004824-39-GB进行中（未招募）1 期
The use of GnRH antagonist versus co-flare protocol for women with low ovarian reserve undergoing first cycle of in vitro fertilization - GnRH-antagonist vs co-flare protocol for women of low ovarian reserve
IVERSITY HOSPITALS OF LEICESTER NHS TRUST0 个研究点目标入组 4 人开始时间: 2014年6月9日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 4
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 23-39 years, with body mass index (BMI) of 19-30 Kg/m2, who are ready to start their first IVF treatment cycle with or without intracytoplasmic sperm injection (ICSI) and who have AMH between 3.08-21.97 pmol/L and day 2-4 serum FSH <15 IU/L. (These AMH levels are compatible with reduced ovarian reserve on Gen II assay results).
- •All women will have 2 ovaries identified on a previous scan.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range: 0
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 60
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range 0
排除标准
- •Previous controlled ovarian stimulation for IVF
- •Day 2-4 serum FSH levels = 15 iu/L
- •AMH > 21.97 or < 3.08 pmol/L
- •Known allergies to study medications
- •Recognised endocrine abnormalities of the hypothalamic pituitary axis such as hypogonadism and hyperprolactinaemia
- •Unsuitable for IVF/ICSI on welfare of the child assessment
- •Concurrent participation in another drug trial
研究者
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