ISRCTN54112208已完成不适用
A study to assess whether complications of anti-coagulation treatment with vitamin K antagonists will diminish by supplementation of vitamin K
etherlands Heart Foundation (Nederlandse Hartstichting) (The Netherlands)0 个研究点目标入组 2,200 人开始时间: 2008年3月31日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 2,200
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
- All
入选标准
- •1. Starting treatment with vitamin K antagonists less then four weeks before inclusion
- •2. Treatment with vitamin K antagonists for a minimal period of six months, with the therapeutic range of International normalised ratio (INR) between 2.5 and 3.5
- •3. Age between 18 and 85 years, either sex
- •4. Measurement of the INR by the Thrombosis Service Leiden
- •5. Informed consent
排除标准
- •1. Treatment for liver failure
- •2. Dialysis, both peritoneal and haemodialysys
- •3. Pregnancy, or wish to get pregnant; lactational period
- •4. Known to have a chronic condition with a life expectancy of less than six months
- •5. An expected interruption of treatment with oral anti-coagulants for one week or longer
- •6. Participation in the self-management protocol
研究者
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