One-Year Results of GENOSS PCB Real-World Study in Femoropopliteal Artery Disease
NCT07431437 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 300
Last updated 2026-02-24
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.
Conditions
- PTA (Percutaneous Transluminal Angioplasty)
- Femoropopliteal Artery Disease
Sponsors & Collaborators
-
Genoss Co., Ltd.
lead INDUSTRY
Eligibility
- Min Age
- 19 Years
- Max Age
- 85 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2025-06-17
- Primary Completion
- 2028-06-30
- Completion
- 2028-06-30
Countries
- South Korea
Study Locations
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