EUCTR2005-002229-30-ES进行中（未招募）1 期
utropin alfa in mid follicular phase in women at risk of poor response suppresed with cetrorelix: an exploratory trial.Lutropina alfa en mitad de la fase folicular en mujeres con riesgo de pobre respuesta en supresión con cetrorelix: estudio exploratorio - Lutropin alfa in risk of poor response.
Serono España, S.A.0 个研究点目标入组 0 人开始时间: 2005年7月11日最近更新:
相关药物
试验速览
- 阶段
- 1 期
- 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
- •1. Pre-menopausal women, aged =38, wishing to conceive.
- •2. Infertility justifying ICSI-TE treatment.
- •3. At risk of poor response criteria due to previous poor response, cancellation of previous cycles or FSH levels.
- •4. Having regular spontaneous menstrual cycle lasting 25-35 days.
- •5. To be included under GnRH antagonist protocol.
- •Are the trial subjects under 18?
- •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)
- •F.1.3.1 Number of subjects for this age range
排除标准
- •1. Known to be HIV, HBV/HCV positive.
- •2. Any clinically significant systemic disease; tumours of the hypotalamus and pituitary gland; ovarian, uterine or mammary cancer; hormonal abnormality and/or medical, biochemical, hematological condition which in the judgement of the investigator may interfere with gonadotropin treatment.
- •3. More than 3 previous ART cycles.
- •4. Cryopreserved embryos from previous cycles with the same partner.
研究者
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