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A study on the safety and efficacy of tirofiban in elderly patients with acute cerebral infarction

A study on the safety and efficacy of tirofiban in elderly patients with acute cerebral infarction

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500115199
Enrollment
Unknown
Registered
2025-12-23
Start date
2025-09-12
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

(Within 24 hours of onset) Acute cerebral infarction, acute ischemic stroke.

Interventions

Experimental group:Intravenous infusion of tirofiban for the first 48 hours
control group:Traditional oral dual antiplatelet therapy: Take aspirin 100 mg daily, clopidogrel 75 mg twice a day, and receive intravenous placebo for 2 days.

Sponsors

Hengzhou People’s Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Age >= 65 years old, able to live and work independently before the onset, acute cerebral infarction occurred within 24 hours after the onset, and NIHSS score >= 2 point ,ands after the onset; 2. CT scan shows that the volume of the intracranial low-density lesion is less than 1/3 of the MCA blood supply area; 3. ASPECTS score >= 3 points (or pc-ASPECTS score >= 6 points); 4. Within 24 hours of onset, there was a progression of symptoms after endovascular treatment (defined as an increase in the NIHSS score from baseline of >= 2 points); 5. Receive intravenous thrombolysis, but if there is no improvement in neurological function within 2 to 24 hours after thrombolysis, it is defined as a decrease in the NIHSS score from the baseline of less than 2 points.

Exclusion criteria

Exclusion criteria: 1. Having a history of severe trauma or stroke within the past three months; 2. Those with intracranial hemorrhage or more than 10 intracranial microbleeds; 3. Patients who are currently taking warfarin; 4. Using thrombolytic drugs within two hours; 5. Patients with definite cardiogenic embolism; 6. Hemorrhagic disorders: Hemophilia, active ulcers, active internal bleeding; 7. Intracranial tumors, cerebral arteriovenous malformations; 8. There is a history of platelet reduction after using tirofiban; 9. Platelet reduction; 10. Allergic constitution; 11. Expected lifespan is less than 90 days.

Design outcomes

Primary

MeasureTime frame
The proportion of patients with a modified Rankin Scale (MRS) score of= 4 points);

Secondary

MeasureTime frame
Intracranial symptomatic and asymptomatic hemorrhage;blood platelet count;The incidence of early neurological deterioration;24-hour improvement rate of HIHSS (reduction of >= 4 points);

Countries

China

Contacts

Public ContactQinian Chen

Hengzhou People’s Hospital

qinianchen@126.com+86 771 6734813

Outcome results

None listed

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