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临床试验/NCT00415792
NCT00415792Unknown4 期

Administration of Human Chorionic Gonadotropin (hCG) Versus Gonadotropin Releasing Hormone (GnRH) Agonist for Ovulation Induction in Hyper-Responder Patients

Eugonia2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2003年11月1日最近更新:
适应症
相关药物

试验速览

阶段
4 期
发起方
入组人数
60
试验地点
2
主要终点
Ongoing pregnancy per embryo transfer

研究概览

简要总结

hCG and GnRH agonist can be used to induce final oocyte maturation and ovulation in IVF cycles. These two approaches will be compared in this study in terms of pregnancy rates and embryological data using patients with hyper-response to IVF drugs.

详细描述

hCG is commonly used for the substitution of the endogenous LH surge to induce oocyte maturation and ovulation induction in ovarian hyperstimulation protocols for in vitro fertilization (IVF). However, hCG is related to the occurrence of the ovarian hyperstimulation syndrome (OHSS), a potentially life-threatening complication and hyper-responding patients are particularly in high risk. An alternative to exogenous hCG is the administration of a GnRH agonist inducing an endogenous rise in both LH and FSH levels due to the initial flare effect.

Comparisons: Pregnancy rates and embryological data will be compared from hyper-responding patients receiving either GnRH agonist (Arvekap) or hCG (Pregnyl) for ovulatrion induction following a GnRH antagonist treatment cycle.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Hyper-responder patients (>20 oocytes retrieved)

排除标准

  • Normal responders
  • Poor responders

结局指标

主要结局

Ongoing pregnancy per embryo transfer

次要结局

  • Embryological data
  • Clinical pregnancy per embryo transfer
  • Biochemical pregnancy per embryo transfer

研究者

发起方
Eugonia
申办方类型
Other

研究点 (2)

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