NCT04539301招募中不适用
Multicentric Prospective Validation of a Universal Test to Quantify Apixaban, Rivaroxaban, Danaparoid and Fondaparinux Levels
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 2,100
- 试验地点
- 1
- 主要终点
- Agreement between measured and estimated levels of each factor-Xa inhibitor
研究概览
简要总结
Despite their usefulness in perioperative and acute care settings, factor-Xa inhibitors-specific assays are scarcely available, contrary to heparin anti-Xa assay. The investigators aimed at assessing whether the widely used heparin anti-Xa assay can quantify the apixaban, rivaroxaban, fondaparinux and danaparoid levels.
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
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- 未提供
排除标准
- 未提供
结局指标
主要结局
Agreement between measured and estimated levels of each factor-Xa inhibitor
时间窗: 2 years
An estimated anticoagulant level between 80 and 120% of the value obtained by the reference method ("specific assay") will be deemed clinically acceptable, i.e. the patient's management would have been the same.
次要结局
- Evaluation of the performance of the estimated anticoagulant level method by an inter-laboratory comparison program(2 years)
- Cost comparison (estimated anticoagulant level method versus specific dosage)(2 years)
研究者
研究点 (1)
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