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Effects of Short-term Intensive Statin Therapy on Lipid Levels

G

General Hospital of Northern Theater Command of Chinese People's Liberation Army

Status

Enrolling

Conditions

Ischemic Stroke

Treatments

Drug: statin

Study type

Observational

Funder types

Other

Identifiers

NCT07344610
Y (2025) 527

Details and patient eligibility

About

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.

Enrollment

800 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 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 criteria

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

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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