LineMatrix® Biological Vascular Graft for Infra-renal Arterial Bypass or Replacement
- Sponsor
- Shanghai Zhongshan Hospital
- Study ID
- NCT07733076
- Status
- Not Yet Recruiting
Notify me when recruiting opens
Save your spot on the interest list for this study. We'll keep your details with this study so our team can follow up when recruiting opens.
Add your contact details and location so we can keep your interest tied to this study.
Conditions
- Peripheral Arterial Disease
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 80 Years
- Healthy Volunteers
- Not accepted
Interventions
- LineMatrix® Biological Vascular Graft — DEVICELineMatrix® Biological Vascular Graft for Infrarenal Arterial Bypass or Replacement
Study Details
Single center, single arm study to evaluate the Safety and Efficacy of LineMatrix® Biological Vascular Graft for Infra-renal Arterial Bypass or Replacement
Key Dates
- First listed
- Jul 29, 2026
- Start date
- Sep 30, 2026
- Status verified
- Jul 2026
- Primary completion
- Sep 30, 2027
- Completion
- Sep 30, 2028
Study Design
- Enrollment
- 15 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: LineMatrix® Biological Vascular Graft
Primary Outcome Measure
Primary patency rate at 6 months postoperatively [ Time Frame: 6 Months ]
Central Contacts
- Weiguo Fu+8613801760929
Related Studies
- FGF-1 for Intramuscular Injection for the Treatment of Peripheral Arterial DiseasePHASE1/PHASE2 · Not Yet Recruiting · Venturis Therapeutics, Inc. · Chicago, Illinois
- Multi-Center Registry for Peripheral Arterial Disease Interventions and OutcomesRecruiting · Baylor Research Institute · Detroit, Michigan
- A Real-World Registry of Chronic Wounds and UlcersRecruiting · U.S. Wound Registry · The Woodlands, Texas
- Ramipril Treatment of Claudication: Oxidative Damage and Muscle FibrosisPHASE4 · Recruiting · University of Nebraska · Omaha, Nebraska