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临床试验/ISRCTN88271422
ISRCTN88271422已完成不适用

The effect of daily low dose mifepristone on the endometrium - study over four consecutive cycles

Medical Research Council (MRC) (UK)0 个研究点目标入组 40 人开始时间: 2000年10月25日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
40

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
Female

入选标准

  • 1. Women aged 18-40 inclusive
  • 2. Regular menstrual cycles
  • 3. Willing and able to take part in the study
  • 4. Prepared to use barrier contraception for the duration of the study
  • 5. Those who are sterilised or whose partner is sterilised
  • 6. Negative serum alpha HCG test before commencing the study (pregnancy test)
  • 7. Written informed consent

排除标准

  • 1. Those who have used hormonal contraception in the past three months, or depot hormones within six months of entering the trial
  • 2. Those who have breastfed in the past three months
  • 3. Those who have had an IUD in situ in the past three months
  • 4. Long term use of any prescription drugs for a significant medical condition
  • 5. History of cervical surgery which may make endometrial biopsy impossible
  • 6. Pregnancy
  • 7. Vaginal bleeding of unknown aetiology or intermenstrual bleeding

研究者

发起方
Medical Research Council (MRC) (UK)

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