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Tirofiban With Sequential Dual Antiplatelet Therapy in Mild Stroke

RecruitingPhase 4Ages 18 Years - 80 YearsAllSecond Affiliated Hospital of Soochow University
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In plain words

What the trial is, and whether it could suit you

This study aims to evaluate whether initiating intravenous tirofiban within 48 hours of onset (with a 48-hour infusion), followed by sequential DAPT, can improve the likelihood of excellent functional outcomes (modified Rankin Scale score 0-1) in mild stroke patients, compared with standard DAPT therapy based on current guidelines.

Sign in to get the eligibility rules as simple questions to take to your doctor.

📋 Eligibility rules (as published)
Inclusion Criteria: 1. Age: 18-80 years old. 2. Acute mild non-cardioembolic stroke. 3. NIHSS score ≤5. 4. Time from onset to randomization of ≤48 hours; if the time of onset is unknown, time from the last known time of being well to randomization of ≤48 hours. 5. The investigational drug can be administered within 48 hours of symptom onset. 6. Signed informed consent by the patient or legally authorized representative. Exclusion Criteria: 1. Received or planned to receive intravenous thrombolysis or bridging therapy (with subsequent endovascular treatment) 2. Intracranial hemorrhage confirmed by imaging. 3. Pre-stroke modified Rankin Scale (mRS) score ≥2. 4. Any confirmed cardioembolic source, including chronic or paroxysmal atrial fibrillation, sick sinus syndrome, mitral stenosis, mechanical heart valve, infective endocarditis, intracardiac thrombus or vegetation, myocardial infarction within 3 months, dilated cardiomyopathy, left atrial spontaneous echo contrast, ejection fraction \<30%. 5. History of primary intracerebral hemorrhage. 6. History of other intracranial hemorrhage (intraventricular, subarachnoid, epidural, or subdural hemorrhage). 7. Untreated or inadequately treated intracranial aneurysm or vascular malformation. 8. Major systemic bleeding within 30 days. 9. Active bleeding, including laboratory evidence of coagulopathy (platelet count \<100 × 10⁹/L, activated partial thromboplastin time \>50 seconds, or international normalized ratio \>1.7), or treatment with direct oral anticoagulants within the preceding 48 hours. 10. Major surgery within 14 days. 11. Persistently elevated blood pressure (systolic \>180 mmHg or diastolic \>110 mmHg) despite treatment. 12. Baseline platelet count \<100 × 10⁹/L. 13. Severe renal dysfunction (glomerular filtration rate \<30 mL/min or serum creatinine \>220 μmol/L \[2.5 mg/dL\]). 14. Known allergy or contraindication to tirofiban or aspirin. 15. Current pregnancy or lactation. 16. Any intracranial tumor (except asymptomatic meningiomas ≤1.5 cm in diameter). 17. Any terminal illness with life expectancy \<6 months.
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What it tests

  • Tirofiban+Oral Dual Antiplatelet Therapy
  • Oral Dual Antiplatelet Therapy
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Where

18 sites
Suzhou Municipal Hospital of Anhui Province
Suzhou, China
Second Hospital of Hebei Medical University
Shijiazhuang, China
Taikang Xian People's Hospital
Zhoukou, China
WuYuan County People's Hospital
Bayan Nur, China
Huai'an First People's Hospital
Huai'an, China
Jiangsu Province (Suqian) Hospital
Suqian, China
Second Affiliated Hospital of Soochow University
Suzhou, China
Affiliated Jiangsu Shengze Hospital of Nanjing Medical University
Suzhou, China

…and 10 more on ClinicalTrials.gov.

🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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