Efficacy of Probucol Combined with Statins Treatment for Ischemic Stroke

RecruitingOBSERVATIONAL
Enrollment

200

Participants

Timeline

Start Date

October 17, 2024

Primary Completion Date

October 31, 2027

Study Completion Date

October 31, 2027

Conditions
Ischemic StrokeAtherosclerosis of ArteryLipid DisorderStatin
Interventions
DRUG

Statin

Participants who opt for this group will receive guideline-recommended conventional lipid-lowering therapy. For those with a history of ischemic stroke (IS), myocardial infarction (MI), acute coronary syndrome within the past year, symptomatic peripheral artery disease, or two or more high-risk factors, the target LDL-C level will be set at 1.4 mmol/L. For other IS participants, the LDL-C target will be set at 1.8 mmol/L. All participants will receive moderate-intensity statin therapy as the primary treatment. If LDL-C levels are not adequately controlled, ezetimibe will be added. If lipid levels remain unsatisfactory, the addition of PCSK9 inhibitors will be considered. Moderate-intensity statins are defined as atorvastatin 10-20 mg or rosuvastatin 5-10 mg.

DRUG

Probucol

Participants who choose this group will receive Probucol in combination with guideline-recommended lipid-lowering therapy. Specifically, participants in this group will take 0.5 grams of Probucol twice daily alongside the conventional lipid-lowering therapy mentioned in Group 1. The combination of Probucol and conventional therapy aims to further improve lipid profile and address atherosclerosis.

Trial Locations (1)

Unknown

RECRUITING

Xuanwu Hospital, Xicheng District

All Listed Sponsors
lead

Xuanwu Hospital, Beijing

OTHER