NCT02894450已完成不适用
Study of Clinical and Laboratory Variables Associated With a Direct Oral Anticoagulant Bioassay (Xaban) Higher Among Those Aged Over 75 Years, as AOD for Atrial Fibrillation
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 70
- 试验地点
- 1
- 主要终点
- bioassay direct oral anticoagulants
研究概览
简要总结
The objective of this study was to investigate whether there is a link between clinical and biological variables and bioassay high xaban in elderly patients as part of an unscheduled hospitalization.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 75 Years 至 —（Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age ≥ 75 years
- •Entering SAU or MPG (Nantes University Hospital) as part of an unscheduled hospitalization for acute or subacute disease (About MPG, will be included patients admitted to the department within 48 hours of calling the doctor)
- •In xaban to entry (dabigatran, rivaroxaban, Apixaban) for non-valvular atrial fibrillation
- •In whom hemostasis tests will be prescribed as part of usual care
- •Patient has given its verbal agreement
排除标准
- •Patients with the following criteria may not be included:
- •Patients refusing to participate in the study
- •Patients under guardianship
- •Inability to obtain the date and time of the last dose of xaban
结局指标
主要结局
bioassay direct oral anticoagulants
时间窗: Baseline
次要结局
未报告次要终点
研究者
研究点 (1)
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