The Impact of Depression and/or Anxiety on Patients With Acute Coronary Syndrome After Percutaneous Coronary Interventions
试验速览
- 阶段
- 不适用
- 入组人数
- 5,000
- 试验地点
- 1
- 主要终点
- Major Adverse Cardiovascular Events
研究概览
简要总结
The purpose of this study is to evaluate how depression and/or anxiety could effect the prognosis of the patients post-ACS after PCI.
详细描述
This trial is a prospective, multi-centric, real-world clinical study. About 5,000 patients with ACS post-PCI will be recruited according to the resource available of each participating center to represent real-world setting. Patients enrolled in the project will accept two-years' follow-up and will be assessed on mortality, cardiovascular events, and severity of depressive or anxiety symptoms using self-rating scales continuously during the trial, in which their treatment for anxiety or depression will also be documented.
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
Major Adverse Cardiovascular Events
时间窗: From date of first visit until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 24 months
death, myocardial infarction, stroke, angina pectoris, revascularization.
次要结局
- Depression self-rating scales(From date of first visit until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 24 months)
- Anxiety self-rating scales(From date of first visit until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 24 months)