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Comprehensive prediction model of antiplatelet therapy for cerebral infarction

Comprehensive prediction model of antiplatelet therapy for cerebral infarction

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500097515
Enrollment
Unknown
Registered
2025-02-20
Start date
2024-05-31
Completion date
Unknown
Last updated
2025-02-24

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

Conditions

Ischemic stroke

Interventions

Aspirin antiplatelet therapy group:None
Clopidogrel antiplatelet therapy group:None
Aspirin clopidogrel dual antiplatelet therapy group:None

Sponsors

Sichuan Academy of Medical Sciences & Sichuan Provice People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Aged 18-80 years; 2.Patients WHO meet the WHO definition of stroke and have non-cardiogenic cerebral infarction confirmed by head CT or MRI; 3.Aspirin and/or clopidogrel antiplatelet drugs for 6-8 days; 4. First onset, the time from onset to admission<=2 weeks; 5.NIHSS score < 15; 6.Informed consent was obtained from patients or their families.

Exclusion criteria

Exclusion criteria: 1.Age 80 years old; 2.Previous medical history/dynamic electrocardiogram/echocardiography/foam test suggested cardiogenic cerebral infarction caused by atrial fibrillation/valvular heart disease/patent foramen ovale, etc. 3.Patients receiving thrombolysis/thrombectomy/stent therapy; 4.Patients taking anticoagulant drugs; 5.Contraindication or intolerance to antiplatelet therapy; 6.Patients with poor compliance and inability to cooperate with the research requirements; 7.Patients or family members refused to sign informed consent forms.

Design outcomes

Primary

MeasureTime frame
Platelet aggregation function;Major ischemic events (ischemic cerebrovascular disease, ischemic cardiovascular disease, peripheral arterial disease, etc.);Major hemorrhagic event (bleeding from the Alliance for Academic Research of Bleeding (BARC) grade 2 or higher);

Secondary

MeasureTime frame
Death or disability;

Countries

China

Contacts

Public ContactYang Jie

Sichuan Academy of Medical Sciences & Sichuan Provice People's Hospital

yangjie1126@163.com+86 136 7813 0516

Outcome results

None listed

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