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临床试验/NCT07569315
NCT07569315尚未招募2 期

Successive Doses of GnRH Agonist Versus Single Dose of GnRH Agonist to Trigger Ovulation in Hyper-responders Undergoing IVF Cycle : A Randomized Controlled Study.

Bedaya Hospital1 个研究点 分布在 1 个国家目标入组 190 人开始时间: 2026年6月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
190
试验地点
1
主要终点
Metaphase-II oocytes rate

研究概览

简要总结

The aim of this randomized controlled study is to compare the efficacy of three successive doses of a GnRH agonist ( administered 36 , 24 and 12 hours before oocyte retrieval ) with a single dose of a GnRH agonist ( administered 36 hours before oocyte retrieval ) in triggering ovulation in hyper-responders

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
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • GnRH antagonist IVF cycle
  • Hyper-responders to induction of ovulation

排除标准

  • Hypogonadotrophic hypogonadism
  • Endometriosis
  • History of recurrent abortion

研究组 & 干预措施

Single dose GnRH agonist

Active Comparator

A single dose of GnRH agonist is administered 36 hours before oocyte retrieval

干预措施: Single dose GnRH agonist (Drug)

Successive doses GnRH agonist

Experimental

Three successive doses of GnRH agonist are administered 36 , 24 and 12 hours before oocyte retrieval

干预措施: Successive doses GnRH agonist (Drug)

结局指标

主要结局

Metaphase-II oocytes rate

时间窗: Ten to fifteen days after starting ovarian stimulation

Number of MII oocyte/ number of cumulus oocyte complex

次要结局

  • Clinical pregnancy rate(Five weeks after embryo transfer)
  • Ongoing pregnancy Rate(Eighteen weeks after embryo transfer)

研究者

发起方
Bedaya Hospital
申办方类型
Other
责任方
Sponsor

研究点 (1)

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