Clinical Trial

Safety and Effectiveness of GENOSS PCB in Patients With Long Femoropopliteal Lesion

Not Yet Recruiting
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Summary
The purpose of this study is to evaluate the long-term safety and efficacy of GENOSS PCB in patients with long femoropopliteal lesions who underwent percutaneous transluminal angioplasty using GENOSS PCB.
Trial Details
NCT Number NCT07425171
Lead Sponsor Genoss Co., Ltd.
Conditions PTA (Percutaneous Transluminal Angioplasty), Femoropopliteal Artery Disease, Long Femoropopliteal Artery Disease
Enrollment 300 participants
Start Date 2026-02-24
Primary Completion 2028-12-31 (estimated)
Study Completion 2028-12-31 (estimated)
Updated on ClinicalTrials.gov 2026-02-20