ISRCTN27244875已完成不适用
Randomised comparison of anticoagulation control and monitoring with versus without laboratory-provided computerized decision support
Ontario Program for Optimal Therapeutics (Canada)0 个研究点目标入组 380 人开始时间: 2005年11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
- 380
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
- •Physicians:
- •1. Family or general practitioner
- •2. Full-time office practice
- •3. Practice address within study laboratory catchment area
- •4. At least 3 eligible patients willing to participate
- •1. On long-term warfarin therapy
- •2. Using the study laboratory for international normalized ratio (INR) tests and expecting to continue to do so for at least 12 months
排除标准
- 未提供
研究者
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