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临床试验/ISRCTN69690272
ISRCTN69690272已完成不适用

A comparison of intrauterine balloon stent and intrauterine contraceptive device in the prevention of adhesion reformation following hysteroscopic surgery for Asherman syndrome: a randomized case-control study

Health Bureau of Zhejiang Province (China)0 个研究点目标入组 200 人开始时间: 2013年2月15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
200

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. Woman with confirmed uterine adhesion with moderate or severe degree [American Fertility Society (AFS score range 5~12)] by hysteroscopic examination and history review for the first time in Sir Run Run Shaw hospital is to be recruited.
  • 2. All the participants should be >=18 years and younger than 40 years old, having potential conceiving requirement

排除标准

  • 1. Older than 40 years old
  • 2. The AFS score less than 5
  • 3. Who doesn't want to get pregnant
  • 4. Who has received hysteroscopic adhesive resection before
  • 5. Who can't follow up according to the study protocol

研究者

发起方
Health Bureau of Zhejiang Province (China)

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