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Vascular Diseases clinical trials

View clinical trials related to Vascular Diseases.

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NCT ID: NCT01454778 Active, not recruiting - Clinical trials for Peripheral Vascular Disease

Paclitaxel Reduces Effects of Intimal Hyperplasia

Pac1
Start date: April 2011
Phase: N/A
Study type: Interventional

This is a single, one time, limited dose infusion of Paclitaxel, that will potentially prevent recurrent stenosis secondary to intimal hyperplasia when compared to the control group at 10 months.

NCT ID: NCT01452165 Completed - Heart Failure Clinical Trials

Peripheral Artery Disease in Vastmanland

PADVa
Start date: May 2006
Phase:
Study type: Observational

The main purposes of this study are: - to describe the prevalence and degree of reduced left ventricular function and hypertrophy in patients with peripheral arterial disease in comparison to controls from the general population, - to evaluate factors of importance to left ventricular dysfunction and hypertrophy in patients with peripheral arterial disease, and - to assess the impact of cardiac function and left ventricular hypertrophy on long-term prognosis in patients with peripheral artery disease.

NCT ID: NCT01447368 Completed - Vascular Diseases Clinical Trials

Cinacalcet Versus Parathyroidectomy in Peritoneal Dialysis Patients

PROCEED
Start date: May 10, 2010
Phase: Phase 4
Study type: Interventional

This is a pilot, prospective randomized controlled study with the primary objective to evaluate and compare medical treatment of severe SHPT, namely oral cinacalcet versus surgical treatment, that is, parathyroidectomy with forearm autografting, on the progression of coronary artery and valvular calcification and left ventricular mass index in endstage renal disease patients receiving peritoneal dialysis over 12 months. The change in arterial stiffening, left ventricular volume, aortic valve calcium score and bone mineral density, nutritional status and biochemical parameters, quality of life measures will be evaluated as secondary objectives of this study.

NCT ID: NCT01444378 Completed - Clinical trials for Peripheral Artery Disease

Absolute Pro® MOMENTUMâ„¢

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

To evaluate the safety and effectiveness of the Absolute Pro® Peripheral Self-Expanding Stent System and the Absolute Pro® LL Peripheral Self-Expanding Stent System for the treatment of subjects with atherosclerotic de novo or restenotic lesions in the native superficial femoral artery (SFA) and/or the native proximal popliteal artery (PPA). CAUTION: Absolute Pro® Peripheral Self-Expanding Stent System and the Absolute Pro® LL Peripheral Self-Expanding Stent Systems are investigational devices. Limited by Federal (U.S.) law to investigational use only.

NCT ID: NCT01429727 Recruiting - Clinical trials for Spontaneous Coronary Artery Dissection

The "Virtual" Multicenter Spontaneous Coronary Artery Dissection (SCAD) Registry

SCAD
Start date: July 2011
Phase:
Study type: Observational

The primary goal of this project is to describe the clinical and physiologic characteristics of Spontaneous Coronary Artery Dissections (SCAD) in order to increase awareness, understanding, treatment and prevention of a potentially fatal cardiovascular event. This study will be a retrospective and prospective review of medical course and current health of men and women with SCAD.

NCT ID: NCT01427179 Enrolling by invitation - Clinical trials for Spontaneous Coronary Artery Dissection

Genetic Investigations in Spontaneous Coronary Artery Dissection (SCAD)

Start date: May 2011
Phase:
Study type: Observational

The purpose of the research is to identify mutations (defects in the genetic blueprint) that cause spontaneous coronary artery dissection (SCAD), in other words, spontaneous tears in blood vessels that supply the heart. Some mutations may be inherited (passed on) from a parent without an apparent blood vessel problem while others may develop for the first time in the affected person.

NCT ID: NCT01424917 Withdrawn - Clinical trials for Cardiac Allograft Vasculopathy

Noninvasive Predictors of Transplant Vasculopathy

CAV
Start date: March 2008
Phase: N/A
Study type: Observational

Post transplant vasculopathy is a major negative outcome in heart transplantation. Current methods of detection are highly invasive and pose a risk to transplant recipients. Noninvasive markers of endothelial function can be used to detect transplant vasculopathy. Endothelial biomarkers such as: endothelial nitric oxide synthase, vascular cellular adhesion molecules, intracellular adhesion molecules, endothelin-1, thromboplastin, circulating endothelial cells, uric acid, and C-reactive play a role in the pathophysiologic mechanism of vasculopathy. Therefore, the investigators would like to assess the association between various endothelial biomarkers and the presence or absence of transplant vasculopathy.

NCT ID: NCT01422343 Withdrawn - Clinical trials for Peripheral Vascular Diseases

Microparticles and the Risk of Re-stenosis Following Balloon Angioplasty in Patients With Peripheral Arterial Disease

Start date: May 2009
Phase: N/A
Study type: Observational

Although microparticles have been well-documented as mediators of inflammation and coagulation in various cardio-vascular disease events, it is currently not known how Percutaneous Transluminal Angioplasty (PTA) for peripheral arterial disease influences microparticle numbers, phenotype and distribution pre- and post interventionally and how they are related to or affect the incidence of early re-stenosis - or if indeed they may be used to predict patients at risk of early re-stenosis.

NCT ID: NCT01418885 Active, not recruiting - Clinical trials for Other Generalized Ischemic Cerebrovascular Disease

Cognitive Impairment , Neuroimaging and Inflammatory Markers in Patients With Subcortical Ischemic Vascular Disease

Start date: September 2010
Phase: N/A
Study type: Observational

SIVD is characterised by extensive cerebral white matter lesions (WML) and lacunar infarcts in deep grey and white matter structures. The relationship between SIVD and cognition is unclear, in part because of methodological inconsistencies across studies. Diffusion tensor imaging (DTI) is a non-invasive water diffusion technique and can be used for quantitatively measuring the degree and directionality of the displacement distribution of water molecules. 1H magnetic resonance spectroscopy (1H-MRS) is a valuable tool for the assessment of several biochemical compounds in the brain in vivo, such as N-acetylaspartate (NAA), myoinositol (mI), Choline (Cho) and Creatine (Cr). There were few reports considering the relationship among MRS, DTI and cognitive impairment of SIVD. Combining MRS with DTI may provide valuable information about the pathophysiological changes underlying DTI abnormalities and help us to better understand the SIVD process. It has been proposed that the pathogenesis of SIVD related to cerebral small vessel disease caused by various mechanisms. Inflammation plays an important role in the pathogenesis of SIVD. The examination of inflammatory markers in relation to VaD might be benefit to early treatment. In this study we applied neuropsychological tests, conventional MRI scanning, DTI, 1H-MRS techniques and inflammatory markers to estimate neuropsychological profile and white matter characteristics of imaging in patients with SIVD. Moreover, the relationship between WML and cognitive function impairment was also investigated. It could be possible to gain reliable data which is benefit to early diagnosis and treatment of cognitive impairment in SIVD.

NCT ID: NCT01418248 Completed - Heart Failure Clinical Trials

Study of Exercise and Heart Function in Patients With Heart Failure and Pulmonary Vascular Disease

EXEC
Start date: August 2011
Phase: N/A
Study type: Observational

Heart Failure with Preserved Ejection Fraction (HFpEF) and Pulmonary Hypertension (PH) can be diagnosed noninvasively by Exercise Echocardiography (ExE) and Cardiopulmonary Exercise Testing (CPX) as compared with gold standard invasive hemodynamic assessment.