NCT07419997招募中不适用
A Multicenter, Retrospective, Observational Cohort Study on Intravenous Thrombolysis Beyond the Time Window for Acute Ischemic Stroke
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 2,600
- 试验地点
- 1
- 主要终点
- Proportion of study participants with mRS scores of 0 - 1
研究概览
简要总结
A multicenter, retrospective, observational cohort study on intravenous thrombolysis beyond the time window for acute ischemic stroke
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Retrospective
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
- •Patients with acute ischemic stroke, regardless of gender;
- •Age ≥ 18 years old;
- •Time from onset to treatment within 4.5 - 24 hours (the onset time refers to the last time when they appeared normal);
- •Complete relevant clinical data (including gender, age, mRS, NIHSS, etc.).
排除标准
- 未提供
研究组 & 干预措施
Alteplase group
The research participants received Alteplase for Acute Ischemic Stroke at 4.5 to 24 Hours
Tenecteplase group
The research participants received Tenecteplase for Acute Ischemic Stroke at 4.5 to 24 Hours
结局指标
主要结局
Proportion of study participants with mRS scores of 0 - 1
时间窗: at 90 (±7) days
Proportion of study participants with mRS scores of 0 - 1
次要结局
- Distribution of mRS scores ranging from 0 to 6(at 90 (±7) days)
- Proportion of study participants with mRS scores of 0 - 2(at 90 (±7) days)
- The proportion of study participants with a NIHSS score of ≤1 or a decrease of ≥8 points compared to the baseline(at 24 (±12) hours)
- mortality rate(at 90 (±7) days)
- Symptomatic intracranial hemorrhage(within 36 hours)
研究者
研究点 (1)
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