JPRN-UMIN000022652已完成未知
Impact of Apixaban on clinical outcome of the patients with Large Vessel Occlusion or stenosis - ALVO trial
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 713
研究概览
简要总结
The cumulative incidence of primary outcome was similar between the two groups. The crude HR of the Early group was 1.19 and the adjusted HR was 1.32 within 365 days.
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 20years-old 至 ot applicable(—)
- 性别
- All
入选标准
- 未提供
排除标准
- •1. Patients who are considered to be ineligible for the study participation by the investigator. 2. Patients who are pregnant or potentially pregnant. 3. Patients who have a history of hypersensitivity to apixaban 4. Patients with hepatic disease having coagulation disorder and clinically important bleeding risk 5. Patients with renal failure (creatinine clearance<15 mL/min) 6. Patients with Active pathological bleeding including intracranial bleeding of any type
研究者
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