Safety and Effectiveness of GENOSS PCB in Patients With Long Femoropopliteal Lesion
NCT07425171 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 300
Last updated 2026-02-20
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.
Conditions
- PTA (Percutaneous Transluminal Angioplasty)
- Femoropopliteal Artery Disease
- Long 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
- 2026-02-24
- Primary Completion
- 2028-12-31
- Completion
- 2028-12-31
Countries
- South Korea
Study Locations
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