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A study on the influencing factors and prognosis of progressive infarction in acute ischemic stroke

A multicenter cohort study on the influencing factors and prognosis of single subcortical infarction, watershed infarction, and arterial to arterial thrombotic infarction in acute ischemic stroke

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500103415
Enrollment
Unknown
Registered
2025-05-29
Start date
2024-01-04
Completion date
Unknown
Last updated
2025-06-02

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

Conditions

Single subcortical stroke, watershed stroke, and arterial to arterial thrombotic stroke within 48 hours of onset

Interventions

Progressive infarction group:None
Non-progressive infarction group:None

Sponsors

The first affiliated hostipal of nanchang university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age >= 40 years old; 2.Admission within 48 hours of onset and completion of first MRI examination (the time of symptom onset is defined as the "last time it appears normal"); 3.Cerebral infarction that meets the following definitions (single subcortical infarction, watershed infarction, arterial to arterial thrombotic infarction, watershed infarction combined with arterial to arterial thrombotic infarction); 4.Signed informed consent form;

Exclusion criteria

Exclusion criteria: 1.Diagnosis of bleeding or other pathological brain disorders based on baseline MRI, such as tumors, abscesses, or other common non ischemic brain disease cases such as multiple sclerosis; 2.Progressive infarction has been made before admission; 3.Pre admission mRS score of 3-5 points; 4.There are contraindications to the use of antiplatelet drugs and statins; 5.There is a risk of using antiplatelet drugs and statins; 6.Received emergency thrombectomy, arterial thrombolysis, and thrombolysis treatment; 7.Suspected cerebral infarction caused by other mechanisms (dissection, moyamoya disease, tumor); 8.Suspected presence of cardioembolic factors such as atrial fibrillation, known artificial heart valves, suspected endocarditis, etc; 9.Cerebral infarction caused by angioplasty/vascular surgery; 10.Severe heart failure (NYHA grade III and IV); 11.Women of childbearing age who have tested negative for pregnancy but refuse to take effective contraceptive measures, as well as pregnant or lactating women; 12.Mental disorders, cognitive or emotional disorders, inability to understand and/or comply with research procedures and/or follow-up; 13.Receiving experimental drug or instrument testing; 14.Due to any reason, the patient cannot be followed up;

Design outcomes

Primary

MeasureTime frame
Progressive cerebral infarction;

Secondary

MeasureTime frame
Progressive cerebral infarction;Progressive cerebral infarction;Changes in neurological disability;quality of life;

Countries

China

Contacts

Public ContactDaojun Hong

The first affiliated hostipal of nanchang university

hongdaojun@hotmail.com+86 791 88692201

Outcome results

None listed

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