NCT05044533已完成不适用
Evaluating QUAlity of Life of AF Patients Following a Bleed (EQUAL-AF)
Bristol-Myers Squibb1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2021年5月31日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 50
- 试验地点
- 1
- 主要终点
- Distribution of characteristics of AF participants: Quality of life (QoL) data
研究概览
简要总结
The purpose of this observational study is to identify participants with both minor and major bleeds as a result of anticoagulant treatment for AF and evaluating their QoL through both primary and secondary care settings.
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
- •Adult patients (>= 18 years old)
- •Patients who can understand all study information and literature to provide fully informed consent
- •Atrial fibrillation (AF) as the primary diagnosis
- •Having a major or minor bleed up to a maximum of 30 days prior to point of enrolment
- •Receiving oral anticoagulation therapy for AF
排除标准
- •Pregnant women
- •Patients with active cancer
- •Patients unable to consent for themselves
- •Patient on concomitant antiplatelet therapy
结局指标
主要结局
Distribution of characteristics of AF participants: Quality of life (QoL) data
时间窗: Up to 90 days
Distribution of characteristics of AF participants: Impact of the anticoagulation treatment
时间窗: Up to 90 days
次要结局
- Distribution of outcomes of AF participants: Timing of bleeding occurrence(Up to 90 days)
- Distribution of outcomes of AF participants: Nature of the bleed(Up to 90 days)
- Distribution of outcomes of AF participants: Documented cause of bleed(Up to 90 days)
- Distribution of outcomes of AF participants: Current Bleeding treatment(Up to 90 days)
- Distribution of outcomes of AF participants: Location of bleed(Up to 90 days)
研究者
研究点 (1)
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