NL-OMON36298已完成不适用
A prospective randomised open label study to determine the best dose escalation scheme of dipyridamol added to acetylsalicylic acid, based on the side-effect headache, in patients starting secondary preventive therapy for stroke - DOSE study
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 114
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
- 年龄范围
- 18 至 99（—）
入选标准
- •age over 18
- •Patients starting treatment with acetylsalicylic acid combined with dipyridamole according to Dutch treatment standards
排除标准
- •Patients not able to start treatment with acetylsalicylic acid combined with dipyridamole according to Dutch treatment standards
研究者
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