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Efficacy and safety of agatreban versus tirofiban in the treatment of progressive stroke

Efficacy and safety of agatreban versus tirofiban in the treatment of progressive stroke

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100049825
Enrollment
Unknown
Registered
2021-08-10
Start date
2021-08-10
Completion date
Unknown
Last updated
2022-04-19

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

Conditions

Progressive stroke

Interventions

Experimental group1:Agartreban is administered intravenously
Experimental group2:Intravenous use of tirofiban
Control group:aspirin+clopidogrel

Sponsors

Nanfang Hospital of Southern Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. All patients met the diagnostic criteria for cerebal infarction in the Chinese Guidelines for the Diagnosis and Treatment of Ischemic Stroke 2018; 2. Progressive stroke patients whose onset was within 6h-1 week and whose NIHSS score increased by at least 1 point. 3. None of them received thrombolytic therapy; 4. First onset or previous onset without obvious sequelae; 5. The patients and their family members signed the informed consent for anticoagulation, anti-plate therapy and DSA.

Exclusion criteria

Exclusion criteria: 1, TIA; 2, cerebral hemorrhage, subarachnoid hemorrhage, hemorrhagic cerebral infarction, brain tumor; 3. Cardiogenic cerebral embolism; 4. Stroke patients with large-scale cerebral infarction or severe consciousness disturbance (NIHSS score 20 points); 5. Complicated with serious heart and lung insufficiency, abnormal liver and kidney function, and diseases of the blood system; 6. Abnormal coagulation function, thrombocytopenia or bleeding tendency, recent (3 months) active bleeding, aortic arch dissection, etc; 7. Tumor patients; 8. Advanced dementia patients; 9. Patients with allergy or allergy to agatreban, tirofiban, antiplatelet drugs.

Design outcomes

Primary

MeasureTime frame
NIHSS;mRS;complication;mortality rate;Barthel Index Rating Table;

Countries

China

Contacts

Public ContactLiang Haiou

Zengcheng Branch of Nanfang Hospital

727786319@qq.com+86 13710990397

Outcome results

None listed

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