Jobst Vascular Institute

Toledo, Ohio 43606

0 studies enrolling now · 20 studies all time

What they study most

Abdominal Aortic Aneurism, Arterial Occlusive Diseases, Arteriovenous Fistula Stenosis, Arteriovenous Graft Stenosis, Bleeding, Carotid Artery Disease, Carotid Artery Diseases, Chronic Venous Insufficiency, Critical Limb Ischemia, Deep Vein Thrombosis, Diabetic Foot Ulcers, Femoral Artery Occlusion

Studies at this site

• Chronic Venous Thrombosis: Relief With Adjunctive Catheter-Directed Therapy (The C-TRACT Trial) — Running, not enrolling
• Post-market, Prospective Evaluation of PHOTO-oxidized Bovine Pericardium in Vascular Surgery — Completed
• Omeza Products in Combination With Standard of Care for the Treatment of Diabetic Foot Ulcers — Completed
• ILLUMENATE Pivotal Post-Approval Study (PAS) — Completed
• Design Validation Hemodynamic Study of New Kendall SCD SmartFlow Compression System — Status unconfirmed
• FLEX Arteriovenous Access Registry — Completed
• The SENTRY Clinical Study — Completed
• An Efficacy and Safety Study of Ixmyelocel-T in Patients With Critical Limb Ischemia (CLI) — Completed
• Pivotal Trial of a Novel Paclitaxel-Coated Percutaneous Angioplasty Balloon — Completed
• Real-World Registry Assessing the Clinical Use of the Lutonix 035 Drug Coated Balloon Catheter — Completed
• Moxy Drug Coated Balloon vs. Standard Balloon Angioplasty for the Treatment of Femoropopliteal Arteries — Completed
• LEVANT 2 Continuation Registry of the Lutonix® Drug Coated Balloon (DCB) — Completed
• VLU Non-Inferiority Study Comparing a Dual Action Pneumatic Compression Device to Multi-Layer Bandaging — Stopped early
• Safety and Efficacy Study for Reverse Flow Used During Carotid Artery Stenting Procedure — Completed
• ENDOvascular Interventions With AngioMAX: The ENDOMAX Trial — Stopped early
• Evaluation of a Dual Action Pneumatic Compression Device: Patient Ease of Use and Comfort — Completed
• A Dose Escalation and Safety Study of Plasmin (Human) In Acute Lower Extremity Native Artery or Bypass Graft Occlusion — Completed
• A Clinical Study to Assess a Compression Device in Patients With Venous Leg Ulcers — Withdrawn before enrolling
• Crux Biomedical Vena Cava Filter Study - United States — Completed
• National Inferior Vena Cava (IVC) Filter Registry — Stopped early