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How short-term intensive statin treatment changes blood fats after ischemic stroke

Observes how statins change cholesterol in adults after ischemic stroke with narrowed arteries.

Plain-language title generated from the registry record
Registry title: Effects of Short-term Intensive Statin Therapy on Lipid Levels

Key facts

Where
Shenyang, ChinaSee the site

Where in China

  • Lu WangShenyang, ChinaTaking people

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Trial details

Who runs it
General Hospital of Shenyang Military Region
Trial code
NCT07344610
Record updated
15 January 2026
Original description
Acute cerebral infarction (ACI), often linked to arterial stenosis, is a major cause of death and disability. Statins are cornerstone therapies for secondary prevention, effectively lowering LDL-C and stabilizing plaques. However, patient response to intensive statin therapy varies significantly. This prospective study aims to analyze the short-term lipid-lowering effects and influencing factors of such therapy in ACI patients with stenosis, to guide personalized treatment and improve outcomes.Read full original descriptionShow less

Effects of Short-term Intensive Statin Therapy on Lipid Levels in Patients With Ischemic Stroke or Large Artery Atherosclerosis: A Prospective Observational Study

Acute cerebral infarction (ACI), often linked to arterial stenosis, is a major cause of death and disability. Statins are cornerstone therapies for secondary prevention, effectively lowering LDL-C and stabilizing plaques. However, patient response to intensive statin therapy varies significantly. This prospective study aims to analyze the short-term lipid-lowering effects and influencing factors of such therapy in ACI patients with stenosis, to guide personalized treatment and improve outcomes.

Inclusion: Age ≥ 18 years; Diagnosis of ischemic stroke (within 14 days of onset) confirmed by cranial CT/MRI; or imaging-confirmed intracranial/extracranial atherosclerotic stenosis (stenosis rate ≥ 50%); Intensive statin therapy (e.g., atorvastatin 40-80 mg/day or rosuvastatin 20 mg/day) initiated within 24 hours of admission, with a planned continuous application for at least one week; Signed informed consent form.

Exclusion: Use of statin therapy within 1 week prior to admission; Receiving other lipid-lowering treatments; Participation in other drug clinical trials within 3 months; Presence of other serious comorbidities (e.g., malignant tumors, end-stage heart failure) with an expected survival of <1 year; Other conditions deemed unsuitable by the investigator; Pregnant or lactating women.

ClinicalTrials.gov NCT07344610