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临床试验/NCT00516490
NCT00516490已完成不适用

GnRH Agonist Administration in the Luteal Phase of ICSI-ET Cycles

V.K.V. American Hospital, Istanbul1 个研究点 分布在 1 个国家目标入组 570 人开始时间: 2006年9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
570
试验地点
1
主要终点
Ongoing pregnancy rate beyond 20 weeks

研究概览

简要总结

A single dose GnRH agonist administration in the luteal phase of assisted reproduction cycles was reported to increase pregnancy and birth rates. This study was done to evaluate the reproducibility of previous findings.

详细描述

GnRH agonist administration in the luteal phase was reported to beneficially affect clinical outcome of ICSI-ET cycles. This randomized controlled trial evaluates the effect of a single dose GnRH agonist administered in the luteal phase on the outcome of ICSI - ET cycles stimulated with the long GnRH agonist protocol. Women undergoing embryo transfer following controlled ovarian hyperstimulation with a long GnRH agonist protocol were included. In addition to routine luteal phase support with progesterone women were randomized to receive a single dose of GnRH agonist or placebo on the sixth day after ICSI.Ongoing pregnancy rate was the primary outcome measure.

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
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Women undergoing embryo transfer following controlled ovarian hyperstimulation with a long GnRH agonist protocol, oocyte pick-up and ICSI.
  • Embryo transfer performed on day 3.

排除标准

  • Participation in another trial that was being conducted in our unit at the same time.
  • Preimplantation genetic screening cycles.
  • Day 5 embryo transfers.

研究组 & 干预措施

1

Experimental

GnRH agonist administration

干预措施: triptorelin acetate (Drug)

2

Placebo Comparator

Sterile saline injection

干预措施: Na Cl %0.9 (Drug)

结局指标

主要结局

Ongoing pregnancy rate beyond 20 weeks

次要结局

  • Embryo implantation rate
  • Clinical pregnancy

研究者

发起方
V.K.V. American Hospital, Istanbul
申办方类型
Other

研究点 (1)

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