Efficacy and Safety Study of Endovascular Treatment of Asymptomatic Carotid Artery Stenosis

NARecruitingINTERVENTIONAL
Enrollment

982

Participants

Timeline

Start Date

October 18, 2024

Primary Completion Date

July 31, 2028

Study Completion Date

July 31, 2028

Conditions
Asymptomatic Carotid Artery Stenosis
Interventions
PROCEDURE

Endovascular treatment

"Participants will receive carotid artery stenting as the primary intervention. The procedure will be performed via femoral artery access (radial access allowed for anatomically challenging cases) with mandatory use of an embolic protection device (EPD). Stent selection and EPD type will be determined by the operator based on lesion characteristics.~Pre-procedural dual antiplatelet therapy (DAPT: aspirin 100 mg/day + clopidogrel 75 mg/day) will be administered for ≥3-5 days. Post-procedural DAPT will continue for 3 months, transitioning to aspirin monotherapy (100 mg/day) thereafter. Statins and risk factor management (blood pressure、LDL-C, glycemic control) will align with standardized protocols."

DRUG

Best medical treatment

Participants will receive intensive medical management, including aspirin (75-325 mg/day) or alternative antiplatelet agents (clopidogrel/dipyridamole) for intolerance. Statin therapy and risk factor control targets (blood pressure, lipids, glucose, lifestyle) will mirror the experimental group. Both groups will undergo regular follow-up for adherence monitoring.

Trial Locations (1)

Unknown

RECRUITING

Beijing Tiantan Hospital, Capital Medical University, Beijing

All Listed Sponsors
lead

Beijing Tiantan Hospital

OTHER