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Brachial Versus Femoral Access for Carotid Artery Stenting

Study acronym: BEFIT
StatusCompleted
PhaseNot applicable
Started2024-09-27
View on ClinicalTrials.gov ↗

Amendment history

2026-09-26
Trial completed
Primary completion confirmed: August 2026 (last estimated December 2026)
2025-07-15
Not Yet Recruiting→Recruiting Study Status, Oversight, Study Design, Contacts/Locations v1
Trial statusNot Yet Recruiting→Recruiting
Primary completion date2025-09→2026-12-31
Completion date2025-12→2026-12-31
Start dateestimated 2024-09→confirmed 2024-09-27
Enrollment target124→226
Study sites0→1
2024-08-13
Original filing
Study purpose: A multicenter, prospective and randomized study is planned to compare the clinical outcomes of carotid artery stenting via brachial artery access and femoral artery access. Eligible participants will be randomly assigned 1:1 to the brachial artery group or the femoral artery group. Primary endpoint: surgical success rate. Secondary endpoints: 1. Operation time (time from first arterial puncture to last angiography) 2. Serious adverse events (SAE) within 90 days; 3. Access puncture complications;
Trial Details
NCT Number NCT06557135
Lead Sponsor The First Affiliated Hospital with Nanjing Medical University
Conditions Carotid Artery Stenosis Without Infarction (Disorder), Ischemic Stroke
Enrollment 235 participants
Start Date 2024-09-27
Primary Completion 2026-08-31 (estimated)
Study Completion 2026-08-31 (estimated)
Updated on ClinicalTrials.gov 2026-09-25