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临床试验/NCT02210611
NCT02210611终止不适用

36 Versus 42 Hour Time Interval From Ovulation Induction to Intrauterine Insemination in Stimulated Cycles With GnRH Antagonists

HaEmek Medical Center, Israel1 个研究点 分布在 1 个国家目标入组 71 人开始时间: 2015年1月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
入组人数
71
试验地点
1
主要终点
Clinical pregnancy rate

研究概览

简要总结

The purpose of this study is to prove that a higher clinical pregnancy rate can be achieved with a 42 to 44 hour time interval between ovulation trigger and intrauterine insemination than a 36 to 38 hour time interval in stimulated cycles utilizing gonadotropins and GnRH antagonists.

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
17 Years 至 44 Years(Child, Adult)
性别
Female
接受健康志愿者

入选标准

  • Patients who can be monitored for follicle growth and hormone measurements on the day of ovulation trigger, or one day before.
  • Patients who have no more than 4 follicles of 14 mm or more
  • Patients who have no more than 6 follicles of 10 mm or more

排除标准

  • Patients who cannot give informed consent to language or comprehension barriers
  • Patients who are deemed to be at high risk for high order multiple gestations
  • Patients who cannot be monitored on the day of hCG administration or one day before

研究组 & 干预措施

36 hours

Active Comparator

Intrauterine insemination 36 hours after ovulation induction

干预措施: Intrauterine Insemination 36 hours (Procedure)

42 hours

Active Comparator

Intrauterine insemination 42 hours after ovulation induction

干预措施: Intrauterine Insemination 42 hours (Procedure)

结局指标

主要结局

Clinical pregnancy rate

时间窗: 4 weeks following insemination

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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