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Clinical Trials in China / NCT07135089
Recruiting Phase 3

Improving Neuroprotective Strategy for Ischemic Stroke Before Endovascular Thrombectomy by Intravenous Tirofiban

NCT07135089 · tracked via the Priya Life Science China tracker
Sponsor
General Hospital of Shenyang Military Region
Phase
Phase 3
Started
2025-11-13
Last updated
2025-12-09

Condition(s) studied

Stroke, Ischemic

Investigational drug(s) / intervention(s)

Intravenous tirofiban before endovascular thrombectomyIntravenous placebo before endovascular thrombectomy

Intravenous tirofiban before endovascular thrombectomy: The tirofiban was administrated as a bolus dose of 10 μg/kg, followed by continuous infusion of 0.15 μg/kg/min for up to 24 hours.

Intravenous placebo before endovascular thrombectomy: The placebo was administrated as a bolus dose of 10 μg/kg, followed by continuous infusion of 0.15 μg/kg/min for up to 24 hours.

Study summary

It remains uncertain whether intravenous tirofiban administered before endovascular thrombectomy could improve disability severity for patients with LVO due to intracranial atherosclerosis.The current study aimed to assess the efficacy and safety of administering intravenous tirofiban before endovascular thrombectomy for improving clinical outcomes in patients with anterior circulation LVO due to intracranial atherosclerosis.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * Age ≥ 18 years; * Anterior circulation large vessel occlusion (the internal carotid artery or the first or second segment of the middle cerebral artery) confirmed by computed tomography angiography (CTA) or magnetic resonance angiography (MRA); * Eligible for endovascular treatment within 12 hours of symptom onset; * Based on the patient's medical history, clinical presentation, and imaging findings, large artery atherosclerosis is highly suspected as the underlying etiology; * Baseline National Institute of Health Stroke Scale (NIHSS) ≥ 6; * Baseline ASPECTS ≥ 6 on CT; * A pre-stroke modified Rankin Scale (mRS) score of ≤2; * Signed informed consent by patient or their legally authorized representative. Exclusion Criteria: * History of atrial fibrillation or atrial flutter, or 12-lead Electrocardiogram before randomization and after admission showing atrial flutter or atrial fibrillation; * Hemorrhagic stroke: cerebral hemorrhage, subarachnoid hemorrhage, or a history of bleeding within one month; * Intracranial aneurysms or malformations, tortuous arteries that hinder thrombectomy, and space-occupying effect brain tumors; * The following drugs are taken within one week: dual antiplatelet drugs, direct oral anticoagulants (DOACs), warfarin and other drugs that increase the risk of bleeding; * Severe uncontrolled hypertension (systolic blood pressure over 200mmHg or diastolic blood pressure over 110 mmHg); * Deficiency of anticoagulant factors or international normalized ratio (INR) \> 1.7, platelet count \< 90×10⁹/L;; * Severe renal insufficiency and advanced disease with an expected life expectancy of less than 6 months; * Pregnancy or lactation; * Allergy to drugs or contrast agents; * Participating in other clinical trials; * Other conditions that the researcher deems unsuitable for participation in this study.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
General Hospital of Northern Theater Command Shenyang Liaoning Recruiting

More General Hospital of Shenyang Military Region trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07135089 on ClinicalTrials.gov ↗ ← All trials in China