跳至主要内容
临床试验/NCT01645241
NCT01645241已完成不适用

Evolutive Potential of Embryos Obtained From Oocytes After Luteal Phase Ovarian Stimulation

Institut Universitari Dexeus1 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2012年7月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
15
试验地点
1
主要终点
Pregnancy rate

研究概览

简要总结

The purpose of this study is to evaluate the clinical pregnancy rate per embryo transfer in oocytes recipients obtained after ovarian stimulation during the luteal phase of oocytes donors . This study will be performed in egg recipients and donors but this type of treatment is meant to be implemented in fertility preservation patients

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 35 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • premenopausal women, 18-35 years old, FSH levels < 10 mIU/ml; AFC> 10
  • regular cycles
  • BMI < 28
  • signed informed consent
  • Recipients:
  • Infertile women eligible for oocytes donation
  • BMI < 35
  • Signed informed consent form

排除标准

  • Polycystic ovarian syndrome, gonadotropins allergy
  • Recipients:
  • Women eligible for oocytes donation
  • Uncontrolled Endocrine Pathology

研究组 & 干预措施

Lutheal phase ovarian stimulation

Experimental

Early luteal phase Controlled ovarian hyperstimulation: we will administer in the 13th-15th cycle day simultaneously 0.25 mg/day of ganirelix to induce luteolysis and FSHr (dose according to BMI and AFC )IU/day for controlled ovarian hyperstimulation until achieving criteria for hCG , to induce final oocyte maturation. Mature oocytes will be vitrified. After warming, oocytes will be inseminated by ICSI with the recipients partners semen sample . Recipient endometrium will be primed with estrogen and progesterone , and embryo transfer will be performed on the 3rd day 3 of embryo cleavage.

干预措施: gonadotropins plus GnRH antagonists (Drug)

Lutheal phase ovarian stimulation

Experimental

Early luteal phase Controlled ovarian hyperstimulation: we will administer in the 13th-15th cycle day simultaneously 0.25 mg/day of ganirelix to induce luteolysis and FSHr (dose according to BMI and AFC )IU/day for controlled ovarian hyperstimulation until achieving criteria for hCG , to induce final oocyte maturation. Mature oocytes will be vitrified. After warming, oocytes will be inseminated by ICSI with the recipients partners semen sample . Recipient endometrium will be primed with estrogen and progesterone , and embryo transfer will be performed on the 3rd day 3 of embryo cleavage.

干预措施: ganirelix (Drug)

结局指标

主要结局

Pregnancy rate

时间窗: six weeks after transfer procedure

次要结局

  • Number of Mature oocytes(Day of oocyte retrieval)

研究者

发起方
Institut Universitari Dexeus
申办方类型
Other

研究点 (1)

Loading locations...

相似试验