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Arterial Occlusive Diseases clinical trials

View clinical trials related to Arterial Occlusive Diseases.

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NCT ID: NCT03339973 Terminated - Clinical trials for Peripheral Arterial Occlusive Disease

Allogeneic ABCB5-positive Stem Cells for Treatment of PAOD

Start date: March 5, 2018
Phase: Phase 1/Phase 2
Study type: Interventional

The aim of this clinical trial is to investigate the efficacy (by monitoring the wound size reduction of Peripheral Arterial Occlusive Disease-related clinically relevant ulcers) and safety (by monitoring adverse events) of one dose of allo-APZ2-PAOD administered intramuscularly into an affected lower leg of patients with Peripheral Arterial Occlusive Disease.

NCT ID: NCT02813577 Terminated - Clinical trials for Femoral Artery Occlusion

Lutonix Drug Coated Balloon for Treatment of Femoropopliteal Arteries in United States Females (CONFIRM)

CONFIRM
Start date: April 20, 2018
Phase: N/A
Study type: Interventional

The post approval study will enroll US female patients presenting with claudication or ischemic rest pain and an angiographically significant lesion in the superficial femoral or popliteal artery. Subjects are treated per Instructions For Use (IFU) with the Lutonix® Catheter. Subjects will have a Duplex Ultrasound (DUS) and clinical follow-up through two (2) years.

NCT ID: NCT02793349 Terminated - Ischemia Clinical Trials

The ABSORB Bioresorbable Scaffold Below the Knee (BTK) Study

Start date: June 2015
Phase: N/A
Study type: Interventional

ABSORB BTK Study: A prospective, multicenter, controlled clinical evaluation of the use of a bioresorbable drug eluting stent in the arterial vasculature below the knee

NCT ID: NCT02699671 Terminated - Clinical trials for Coronary Artery Disease

IRIS-BVS AMI Registry

IRIS BVS AMI
Start date: June 2016
Phase:
Study type: Observational

The purpose of this study is to evaluate the relative effectiveness and safety of Bioresorbable Vascular Scaffold in acute myocardial infarction compared to other (drug eluting stents) DES.

NCT ID: NCT02622100 Terminated - Clinical trials for Coronary Artery Disease

Evaluation of Effectiveness and Safety of Bioresorbable Vascular Scaffold in Routine Clinical Practice

IRIS BVS
Start date: February 26, 2016
Phase:
Study type: Observational

The purpose of this study is to evaluate the relative effectiveness and safety of Bioresorbable Vascular Scaffold compared to other (drug eluting stents) DES.

NCT ID: NCT01601496 Terminated - Clinical trials for Peripheral Arterial Occlusive Disease (PAOD)

Evaluation of FUSION™ Vascular Graft for Above Knee Targets

PERFECTION
Start date: October 26, 2009
Phase: N/A
Study type: Interventional

The purpose of the post-market study was to evaluate the safety and performance of the FUSION Vascular Graft.

NCT ID: NCT01520311 Terminated - Clinical trials for Coronary Artery Disease

The eSVS® Mesh Post-Marketing Trial

Start date: January 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate patency rates of the eSVS Mesh Saphenous Vein Graph (SVG) and control SVG at six and twenty-four months via coronary angiography and analyses of Duplex Sonography Results and coronary angiography and major cardiovascular or cerebrovascular event (MACCE)-Rate as well as analysis of preoperative great saphenous vein (GSV) duplex sonography and intra-operative GSV harvesting findings and procedure.

NCT ID: NCT01462721 Terminated - Clinical trials for Coronary Artery Disease

The eSVS® Mesh Randomized Post-Market Study

Start date: October 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate patency rates of the external Saphenous Vein Support (eSVS) Mesh Saphenous Vein Grafts (SVG) and Control SVG at 3-6 months and 24 months.

NCT ID: NCT01341340 Terminated - Atherosclerosis Clinical Trials

The ABSORB BTK (Below The Knee) Clinical Investigation

Start date: November 2011
Phase: N/A
Study type: Interventional

The purpose of the ABSORB BTK Clinical Investigation is to evaluate the safety and efficacy of the Everolimus Eluting Bioresorbable Vascular Scaffold System (BVS) in subjects with critical limb ischemia (CLI) following percutaneous transluminal angioplasty (PTA) of the tibial arteries.

NCT ID: NCT00940979 Terminated - Clinical trials for Arterial Obstructive Diseases

Trial Using Integuseal as Microbial Sealant for Arterial Bypass Surgery on Lower Extremities

ITT
Start date: January 2010
Phase: N/A
Study type: Interventional

The purpose of this study is to prove a reduction of postoperative wound infections after direct preoperative use of a microbial sealant in the form of Integuseal for vascular procedures on lower extremities.