NCT03444012已完成不适用
Non-interventional Prospective Data Collection on Persistence and Adherence on Ticagrelor in ACS Adult Patients in Serbia
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- AstraZeneca
- 入组人数
- 269
- 试验地点
- 9
- 主要终点
- duration (number of days) on ticagrelor therapy in patients with acute coronary syndrome
研究概览
简要总结
noninterventional study investigating persistence and adherence on ticagrelor in ACS patients in Serbia
研究设计
- 研究类型
- Observational
- 观察模型
- Other
- 时间视角
- Cross Sectional
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
- •≥ 18 years of age
- •diagnosed with ACS - STEMI or NSTEMI or unstable angina, invasively or non-invasively treated
- •Patients already on treatment with ticagrelor at least for 1 month and no longer than 3 months prior to study initiation. Enrolment in this study must not be trigger for ticagrelor initiation.
- •read and signed the Informed Consent Form
排除标准
- •Any contraindications as per approved SmPC of Brilique
- •Patients with life-threatening conditions which could disable patients to comply with scheduled visits and/or not able to fill in the patient questionnaires.
结局指标
主要结局
duration (number of days) on ticagrelor therapy in patients with acute coronary syndrome
时间窗: 1 year (12 months)
次要结局
未报告次要终点
研究者
研究点 (9)
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