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Peripheral Vascular Diseases clinical trials

View clinical trials related to Peripheral Vascular Diseases.

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NCT ID: NCT00895635 Completed - Clinical trials for Intermittent Claudication

Evaluating Two Exercise Training Programs to Reduce Leg Pain in People With Peripheral Arterial Disease (The EXERT Study)

EXERT
Start date: January 2009
Phase: Phase 3
Study type: Interventional

Peripheral arterial disease (PAD) is a disorder that affects more than 8 million people in the United States. As a result of decreased blood flow to the legs, people with PAD may experience leg pain and difficulty with walking. This study will examine the effectiveness of two exercise programs—a treadmill walking program and an aerobic arm exercise program—at increasing walking distance and decreasing leg pain in people with PAD.

NCT ID: NCT00883246 Completed - Clinical trials for Peripheral Arterial Disease

Study of SilverHawk®/TurboHawk® in Lower Extremity Vessels (DEFINITIVE™ LE)

Start date: April 2009
Phase: N/A
Study type: Interventional

The purpose of the study is to evaluate the intermediate and long-term effectiveness of stand-alone atherectomy treatment of peripheral arterial disease in the legs.

NCT ID: NCT00879697 Completed - Hypertension Clinical Trials

Strength Training in Walking Tolerance in Intermittent Claudication Patients

Start date: July 2005
Phase: Phase 3
Study type: Interventional

Background: Muscle atrophy and reduced leg strength are related to exercise intolerance in patients with intermittent claudication (IC), suggesting that strength training (ST) could improve exercise performance in these patients. Objective: Analyze the effects of ST in walking capacity in patients with IC comparing with walking training (WT) effects. Intervention: Patients were randomized into ST and WT. Both groups trained twice a week, for 12 weeks, at the same rate of perceived exertion. ST consisted of 3 sets of 10 repetitions of whole body exercises. WT consisted of 15 two-minute bouts of walking intercalated with 2 minutes of resting. Measurements: Walking capacity, peak VO2, walking economy, ankle brachial index, ischemic window and knee extension strength

NCT ID: NCT00872326 Completed - Diabetic Foot Clinical Trials

Autologous Bone Marrow Derived Mononuclear Cells in Treating Diabetic Patients With Critical Limb Ischemia

Start date: December 2007
Phase: Phase 1/Phase 2
Study type: Interventional

The aim of this study is to assess the efficacy and safety of autologous transplantation of bone-marrow cells for therapeutic angiogenesis and vasculogenesis in diabetic patients with non-revascularizable critical limb ischemia.

NCT ID: NCT00862420 Completed - Clinical trials for Peripheral Arterial Disease (PAD)

Safety Evaluation of Clopidogrel Sulfate in Patients With Peripheral Arterial Disease

Start date: February 2009
Phase: Phase 3
Study type: Interventional

Primary objective: - To evaluate whether 12 weeks of clopidogrel is superior to ticlopidine in terms of lower risk of the safety events of interests in patients with peripheral arterial disease (PAD) Secondary objectives: - To compare the risk of bleeding adverse events, serious adverse events and overall safety of clopidogrel with ticlopidine - To compare the risk of vascular events of clopidogrel with ticlopidine - To document the long-term safety of clopidogrel for a total of 52 weeks - To document the vascular events of clopidogrel for a total of 52 weeks

NCT ID: NCT00855673 Completed - Clinical trials for Peripheral Arterial Disease

Intermittent Mechanical Compression For Peripheral Arterial Disease

FM-S1
Start date: January 2001
Phase: Phase 4
Study type: Interventional

The study tests the use of a portable mechanical compression device (FM220, Flowmedic, USA) for the treatment of claudication and peripheral arterial disease. Major endpoints are improved exercise tolerance and relevant blood pressure ratios

NCT ID: NCT00844532 Completed - Clinical trials for Peripheral Vascular Disease

Trial to Evaluate the Safety & Efficacy of the Absolute Pro™ Peripheral Self-Expanding Stent System in Subjects With Atherosclerotic de Novo or Restenotic Lesions in the Native Common Iliac Artery and/or Native External Iliac Artery.

MOBILITY AP
Start date: March 2009
Phase: Phase 3
Study type: Interventional

To determine the safety and efficacy of the Absolute Pro™ Peripheral Self-Expanding Stent System in subjects with atherosclerotic de novo or restenotic lesions in the native common iliac artery and/or native external iliac artery.

NCT ID: NCT00837954 Completed - Clinical trials for Peripheral Vascular Diseases

Trial to Evaluate the Hemostatic Effect of Lyostypt® Versus Surgicel® in Arterial Bypass Anastomosis

COBBANA
Start date: February 2009
Phase: Phase 4
Study type: Interventional

The purpose of this trial is to demonstrate that the bleeding time of suture holes after construction of arterial bypass anastomosis is shorter after treatment with Lyostypt® than with Surgicel®

NCT ID: NCT00831090 Completed - Clinical trials for Cardiovascular Disease

Endothelial Function and Vein Graft Remodeling

EFVGR
Start date: January 2009
Phase:
Study type: Observational

The purpose of this study is to better understand why some vein bypass grafts develop narrowing. Evidence suggests that there is a relationship between inflammatory markers in the blood and the narrowing that occurs in blood vessels. In this study, we will look at inflammatory markers in the blood and how well the vein graft functions.

NCT ID: NCT00827853 Completed - Clinical trials for PERIPHERAL VASCULAR DISEASE

Study Comparing Two Methods of Expanding Stents Placed in Legs of Diabetics With Peripheral Vascular Disease

COBRA
Start date: November 2008
Phase: N/A
Study type: Interventional

Despite recent advances in stent technology and its widespread application in the treatment of peripheral vascular disease (PVD), incidences of partial or complete blockage of stent lumen (in-stent restenosis) due to in growth of cells (neo-intimal proliferation) is unacceptably high. In diabetics with long superficial femoral artery (SFA) lesions, in-stent restenosis rates are higher than in non-diabetics. Consequently interventional techniques that curtail in-stent restenosis have to be explored. Cryoplasty is a stent expansion method in which a balloon is expanded using pressurized nitrous oxide gas. As the nitrous oxide expands in the balloon it cools the surroundings to about -10 degrees C. This induces programed death (apoptosis) of the smooth muscle cells in arterial wall. The investigators hypothesize that Cryoplasty, by inducing an apoptotic smooth muscle cell response, when applied to post-dilation of nitinol self-expanding stents in the Superficial Femoral Artery (SFA) of diabetics, would lead to decreased in-stent restenosis due to decreased neointimal proliferation.