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Vascular Diseases clinical trials

View clinical trials related to Vascular Diseases.

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NCT ID: NCT00764270 Active, not recruiting - Atherosclerosis Clinical Trials

The Role of R-Alpha Lipoic Acid in the Treatment of Atherosclerotic Vascular Disease

Start date: August 2011
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to see if a dietary supplement, R-alpha lipoic acid, is able to reduce risk factors in people with documented heart disease and increased levels of inflammation.

NCT ID: NCT00471289 Active, not recruiting - Clinical trials for Peripheral Vascular Disease

PTA and Drug Eluting Stents for Infrapopliteal Lesions in Critical Limb Ischemia

PADI
Start date: August 2007
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to investigate the performance of paclitaxel-coated balloon expandable stainless steel coronary stent for the treatment of infrapopliteal stenoses and occlusions in patients with critical limb ischemia compared to percutaneous transluminal balloon angioplasty (PTA).

NCT ID: NCT00449306 Active, not recruiting - Atherosclerosis Clinical Trials

Physical,Histological,and Genetic Analyses of Lipid-rich Atherosclerotic Plaques

Start date: March 2001
Phase:
Study type: Observational

Lipid-rich atherosclerotic plaques, or "vulnerable plaques" are prone to rupture, causing local intravascular thrombosis, with subsequent grave clinical consequences. Atherosclerotic plaques normally removed during surgery, and peripheral blood samples will be studied to achieve the following objectives: "1" Define histological features of the vulnerable plaque, analyze its physical characteristics, and investigate selected gene expression. "2" Study biomarkers of inflammation in conjunction with the presence of vulnerable plaques. "3" Explore the potential role of infection in atherogenesis.

NCT ID: NCT00434616 Active, not recruiting - Diabetic Foot Clinical Trials

Autologous Bone Marrow Stem Cell Transplantation for Critical, Limb-threatening Ischemia

BONMOT
Start date: April 2007
Phase: Phase 2/Phase 3
Study type: Interventional

Critical limb ischemia is a condition where the blood circulation in the limbs, in most cases the legs, is decreased so that pain and non healing wounds ensue. Mostly, this is a sequel of arteriosclerosis and/or diabetes. If surgical and other methods for the improvement of blood supply for the leg have failed or are not possible, most of these patients will proceed to amputation of the leg. Bone marrow contains cells which can induce and augment the growth of new, small arteries called collateral arteries. It has been shown in animals and in some case series that the transplantation of a concentrate of the patient's own bone marrow with stem cells into the ischemic limb can improve the blood circulation via the induction of collateral growth. However, it is not known if this bone-marrow stem cell induced collateral growth is sufficient to avoid otherwise necessary amputations. Therefore, we conduct a study to compare the efficiency of concentrated bone marrow cells injected into the critically ischemic limb compared to a placebo procedure where only saline is injected. We think that the transplantation of autologous bone marrow will reduce the number of necessary leg amputations, reduce pain and induce wound healing. In this investigation, patients with limb threatening ischemia are randomly allocated either to the bone marrow group or to the placebo group. Patients in the bone marrow group will have their bone marrow harvested under sedation, and the bone marrow cells are concentrated. The cell concentrate will then be injected directly into the muscle of the diseased leg. Patients in the placebo group will undergo sedation as well but no bone marrow harvest is done, and saline is injected into the ischemic leg. The procedure will require about 1.5-2 hours, and the subjects will be admitted to a participating vascular Centre. Monthly examinations up to three months after the bone-marrow or placebo procedure are done. After the follow-up of three months, the rate of death and amputations and the wound healing process are compared between groups. Adverse and serious adverse events will be recorded during this time period. Diagnostic studies will be obtained to measure blood flow in the treated leg during the follow up period and include skin oxygen measurements, pressure recordings in the leg and arteriography. Also, quality of life, pain and wound healing will be assessed. After completion of the three months study participation, subjects who have been treated with placebo will be able to receive open-label bone marrow transplantation therapy.

NCT ID: NCT00344617 Active, not recruiting - Clinical trials for Polypoidal Choroidal Vasculopathy

Off-Label AVASTIN (BEVACIZUMAB) For Serosanguinous Maculopathy

Start date: June 2006
Phase: Phase 3
Study type: Interventional

To assess the use of Avastin for the management of serosanguinous maculopathy

NCT ID: NCT00251849 Active, not recruiting - Clinical trials for Intermittent Claudication

PROVIDENCE-1: Study of Rifalazil in Chlamydia Pneumoniae Seropositive Patients

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

The objective of this study is to determine whether rifalazil can significantly increase peak walking time (PWT) in patients with peripheral arterial disease (PAD).

NCT ID: NCT00132743 Active, not recruiting - Clinical trials for Cardiovascular Diseases

Claudication: Exercise Versus Endoluminal Revascularization (CLEVER)

CLEVER
Start date: February 2007
Phase: Phase 3
Study type: Interventional

The purpose of this study is to compare the effectiveness of aortic stent surgery versus exercise therapy in individuals with aortoiliac insufficiency.

NCT ID: NCT00125671 Active, not recruiting - Clinical trials for Cardiovascular Diseases

Warfarin and Antiplatelet Vascular Evaluation

Start date: January 2000
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate whether the addition of warfarin (a blood-thinning medication) to an antiplatelet therapy like aspirin is better than antiplatelet therapy alone (i.e. usual treatment) for the prevention of leg surgery, heart attacks, stroke and death in people with peripheral vascular disease.

NCT ID: NCT00123227 Active, not recruiting - Hypertension Clinical Trials

Rosiglitazone Plaque Study

Start date: October 2002
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether rosiglitazone, a peroxisome proliferator activated receptor gamma (PPAR-gamma) agonist, induces regression in carotid atherosclerotic plaques in diabetic patients with vascular disease and/or hypertension over a 12 month period.