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临床试验/ACTRN12614000626662
ACTRN12614000626662已完成未知

A randomised controlled trial assessing the effect of endometrial pipelle biopsy vs. no intervention on live birth rate in women undergoing autologous embryo transfer.

Auckland District Health Board0 个研究点目标入组 1,300 人开始时间: 2014年6月13日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
1,300

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Open (masking not used)

入排标准

年龄范围
18 Years 至 o limit(—)
性别
Female

入选标准

  • Women planning to undergo autologous embryo transfer with any indication of subfertility

排除标准

  • 1. Have had any disruptive instrumentation within the uterine cavity (e.g. hysteroscopy, hysterosalpingogram, laparoscopy, surgically managed miscarriage or endometrial biopsy) within three months prior to day one of the planned embryo transfer cycle, or planning to undergo a procedure involving disruptive instrumentation at any stage during the study. Embryo transfer and intrauterine insemination procedures are not considered to cause disruptive instrumentation
  • 2. Entered previously into this study or participation in another trial in the last 30 days
  • 3. Any contraindication to endometrial biopsy, being pregnant and/or carrying a pregnancy to term
  • 4. Not planning an embryo transfer (e.g. fertility preservation or planned freeze-all cycles)

研究者

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