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临床试验/JPRN-UMIN000022652
JPRN-UMIN000022652已完成未知

Impact of Apixaban on clinical outcome of the patients with Large Vessel Occlusion or stenosis - ALVO trial

Hyogo college of medicine0 个研究点目标入组 713 人开始时间: 2016年6月8日最近更新:
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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