Clinical Outcomes of GENOSS PCB for Femoropopliteal Artery Disease
NCT07399080 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 200
Last updated 2026-02-18
Summary
The GENOSS PCB study aims to evaluate the safety and efficacy of a Paclitaxel-coated PTA Balloon Catheter(GENOSS® PCB) in patients with the 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
- 2025-07-01
- Primary Completion
- 2028-06-30
- Completion
- 2028-06-30
Countries
- South Korea
Study Locations
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