EUCTR2007-006443-50-BE进行中（未招募）不适用
Prospective, randomized trial to evaluate the administration of 2 different doses of recombinant FSH to patients with age depended insufficient ovarian response during IVF/ICSI
niversity Hospital Ghent0 个研究点开始时间: 2007年11月21日最近更新:
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
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 > 38 years, who had insufficient response to stimulation with regular (for that age) posology of 225 IU of gonadotrophins (urinary or recombinant), in a short agonist protocol in a previous cycle
- •Insufficient response is defined as: development of < or = 4 mature follicles (of > or = 16 mm) at time of hCG administration.
- •- Patient can be eligible for several cycles in the same protocol
- •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
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •- Patients who received already doses > 225 IU, whatever the outcome was
- •- Patients older than 43 years
- •- Patients with basal FSH concentrations > or = 15 mU/ml at Day 3
研究者
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