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

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

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500113387
Enrollment
Unknown
Registered
2025-11-27
Start date
2025-12-01
Completion date
Unknown
Last updated
2025-12-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ischemic stroke

Interventions

Tirofiban group:Patients will receive intravenous tirofiban before endovascular treatment(0.4 µg/kg/min, intravenous infusion within 30 minutes, and 0.1 µg/kg/min intravenous infusion for 23.5 hours).
Placebo group:Patients will receive intravenous placebo before endovascular treatment(0.4 µg/kg/min, intravenous infusion within 30 minutes, and 0.1 µg/kg/min intravenous infusion for 23.5 hours).

Sponsors

General Hospital of Northern Theater Command
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >= 18 years; 2. Time from onset to randomization between 4.5 and 12.0 hours; 3. Preliminary diagnosis of anterior circulation ischemic stroke based on clinical symptoms or imaging; 4. National Institutes of Health Stroke Scale (NIHSS) score = 6; 6. Computed Tomography Angiography (CTA) / Magnetic Resonance Angiography (MRA) / Digital Subtraction Angiography (DSA) confirms occlusion of the intracranial segment of the internal carotid artery and the M1/M2 segments of the middle cerebral artery, and endovascular treatment is decided; 7. The patient or their family signs a written informed consent form.

Exclusion criteria

Exclusion criteria: 1. Age >= 18 years old; 2. Time from onset to randomization between 4.5 and 12.0 hours; 3. Preliminary diagnosis of anterior circulation ischemic stroke based on clinical symptoms or imaging examination; 4. National Institutes of Health Stroke Scale (NIHSS) score = 6 points; 6. Intracranial aneurysms or malformations, arterial tortuosity obstructing thrombectomy, space-occupying brain tumors.

Design outcomes

Primary

MeasureTime frame
Proportion of mRS 0-2 at 90 days;

Secondary

MeasureTime frame
90-day mRS score 0-1 or recovery to pre-stroke mRS score (%);Distribution of 90-day mRS scores;the proportions of patients with substantial reperfusion at initial preprocedure catheter angiogram ;DSA vascular recanalization success rate before the end of endovascular treatment;Postoperative 24h CTA/MRA vessel recanalization success rate;Change in NIHSS score 24 hours post-surgery;Changes in NIHSS scores 10 days after surgery;Occurrence of cardiovascular and cerebrovascular events within 90 days after surgery;

Countries

China

Contacts

Public ContactChen Huisheng

General Hospital of Northern Theater Command

chszh@aliyun.com+86 133 5245 2086

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026