Early Low-dose ASpirin Use After Intravenous Thrombolysis for Acute Ischemic Cerebral Infarction(ELASTIC) (ELASTIC)
2026年5月5日 更新者:Beijing Chao Yang Hospital
Safety and Efficacy of Treatment With Early Low-dose ASpirin Use After Intravenous Thrombolysis for Acute Ischemic Cerebral Infarction (ELASTIC): A Randomized, Open-label, Blinded Endpoint, Clinical Trial
This study evaluates whether early administration of low-dose aspirin (100mg) at 2 hours post-intravenous thrombolysis, compared to the standard timing of 24 hours, improves functional outcomes in patients with acute ischemic stroke.
Intravenous thrombolysis is effective for very early treatment of acute ischemic stroke.
However, current guidelines recommend starting antiplatelet therapy 24 hours after thrombolysis to avoid symptomatic intracranial hemorrhage (SICH), a recommendation not based on prospective clinical studies.
Early re-occlusion of recanalized arteries due to platelet aggregation occurs in 14-34% of cases and is associated with poor prognosis.
The average incidence of SICH is 2.4%, with fatal SICH occurring in only 0.28%.
Thus, the impact of re-occlusion on poor prognosis may outweigh the risk of SICH.
In this prospective, randomized, open-label trial with blinded endpoint evaluation, participants are assigned to receive aspirin 100mg either at 2 hours (early group) or at 24 hours (standard group) after thrombolysis.
The primary outcome is the proportion of patients with a favorable functional outcome, defined as a modified Rankin Scale (mRS) score of 0-2 at 3 months.
Safety outcomes include the incidence of SICH and all-cause mortality at 3 months.
This study will provide clinical evidence regarding the optimal timing for initiating antiplatelet therapy after thrombolysis in acute ischemic stroke.
研究概览
研究类型
介入性
注册 (估计的)
210
阶段
- 第四阶段
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习联系方式
- 姓名:Ming Lu, MD
- 电话号码:010-8523-1391
- 邮箱:brian0317@sina.com
学习地点
-
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Beijing Municipality
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Beijing、Beijing Municipality、中国、100020
- Beijng Chao-Yang Hospital, Capital Medical University
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参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
不
描述
Inclusion Criteria:
- Age range: 18-65 years old
- Receive rt PA thrombolytic therapy within 3 hours (including 3 hours) of onset
- Signs of brain dysfunction lasting for more than 1 hour
- CT imaging excludes cerebral hemorrhage, and there are no imaging changes corresponding to the patient's physical signs
Exclusion Criteria:
- Age>65 years old
- Onset time>3 hours
- Accompanied by consciousness disorders, or NIHSS ≥ 20 points
- CT shows' high-density shadow of middle cerebral artery '
- Accompanied by atrial fibrillation or clearly identified as cardioembolic embolism
- Severe swallowing difficulties, unable to take medication orally
- Oral anticoagulant medication is currently being taken
- Accompanied by severe infection or evidence of severe infection
- Refusal to sign the informed consent form for this study
- Exclusion criteria for other traditional intravenous thrombolysis
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:Early Aspirin Group
Participants receive oral aspirin 100mg at 2 hours after rt-PA thrombolysis.
A follow-up CT scan is performed at 2 hours post-thrombolysis.
If no intracranial hemorrhage is confirmed, aspirin 100mg once daily (Qd) is continued for 3 months.
|
Aspirin 100mg orally, administered once daily.
The first dose is given at 2 hours after rt-PA thrombolysis, conditional on a follow-up CT scan at 2 hours excluding intracranial hemorrhage.
Treatment continues for 3 months.
|
|
有源比较器:Standard Therapy Group
Participants receive oral aspirin 100mg once daily (Qd) starting at 24 hours after rt-PA thrombolysis.
A follow-up CT scan is performed at 24 hours post-thrombolysis.
If no intracranial hemorrhage is confirmed, aspirin 100mg once daily (Qd) is continued for 3 months.
|
Aspirin 100mg orally, administered once daily.
The first dose is given at 24 hours after rt-PA thrombolysis, conditional on a follow-up CT scan at 24 hours confirming no intracranial hemorrhage.
Treatment continues for 3 months.
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Proportion of Patients with Favorable Functional Outcome at 3 Months
大体时间:3 months
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Favorable functional outcome is defined as a score of 0 to 2 on the modified Rankin Scale (mRS).
The mRS score will be assessed by a blinded endpoint assessor at 3 months post-stroke via a structured telephone interview or during a clinic visit.
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3 months
|
次要结果测量
结果测量 |
大体时间 |
|---|---|
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Incidence of symptomatic intracranial hemorrhage
大体时间:24 hour
|
24 hour
|
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Patient mortality rate at 3 months
大体时间:3 months
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3 months
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合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (估计的)
2026年5月1日
初级完成 (估计的)
2027年9月30日
研究完成 (估计的)
2027年12月31日
研究注册日期
首次提交
2026年4月26日
首先提交符合 QC 标准的
2026年4月26日
首次发布 (实际的)
2026年5月4日
研究记录更新
最后更新发布 (实际的)
2026年5月8日
上次提交的符合 QC 标准的更新
2026年5月5日
最后验证
2026年4月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.