Clinical Trial

One-Year Results of GENOSS PCB Real-World Study in Femoropopliteal Artery Disease

Enrolling by Invitation
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Summary
The purpose of this study is to evaluate the long-term safety and efficacy of GENOSS PCB by enrolling and tracking patients who underwent percutaneous transluminal angioplasty using GENOSS PCB in patients with femoropopliteal artery disease.
Trial Details
NCT Number NCT07431437
Lead Sponsor Genoss Co., Ltd.
Conditions PTA (Percutaneous Transluminal Angioplasty), Femoropopliteal Artery Disease
Enrollment 300 participants
Start Date 2025-06-17
Primary Completion 2028-06-30 (estimated)
Study Completion 2028-06-30 (estimated)
Updated on ClinicalTrials.gov 2026-02-24