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Vascular Diseases clinical trials

View clinical trials related to Vascular Diseases.

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NCT ID: NCT00822172 Completed - Clinical trials for Peripheral Arterial Disease

Evaluation of Cilostazol in Combination With L-Carnitine

ECLECTIC
Start date: September 2008
Phase: Phase 4
Study type: Interventional

The purpose of this study is to see how safe and effective L carnitine taken with cilostazol is compared to placebo taken with cilostazol for people with intermittent claudication. A second purpose of the study is to see if L-carnitine is absorbed into the blood stream.

NCT ID: NCT00820378 Recruiting - Hypertension Clinical Trials

The Epidemiology of Aortic Diameter in China

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

Aortic aneurysms are the major disease processes affecting the aorta and becoming a relatively common cause of death because of rupture or dissection. The most common location for aneurysms is the infrarenal abdominal aorta, followed by the ascending thoracic aorta. Unlike coronary heart disease, the incidence of abdominal aortic aneurysm (AAA) in the United States and Europe has been increasing, and this increase may not be due to higher levels of screening for this condition alone. Aortic diameter is central to the diagnosis of aortic aneurysm. Furthermore, it was demonstrated that non-AAA patients with an enlarged diameter of the infrarenal aortic diameter are also at high risk for all-cause mortality. And aortic root dimension was associated with several coronary artery disease (CHD) risk factors and measures of subclinical disease and was predictive of incident congestive heart failure (CHF), stroke, cardiovascular disease (CVD) mortality, and all-cause mortality, but not of incident MI. Up to now, there are limited studies on the epidemiology of aortic diameter, especially in Chinese population.

NCT ID: NCT00817349 Completed - Clinical trials for Coronary Artery Disease

Angio-Seal Evolution Device Registry

Start date: July 2008
Phase:
Study type: Observational

Collect data on the use of the Angio-Seal Evolution Device in diagnostic and interventional patient populations.

NCT ID: NCT00814970 Completed - Clinical trials for Peripheral Vascular Disease

The Complete® SE SFA Study for the Treatment of SFA/PPA Lesions

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

To evaluate the safety and efficacy of the Complete SE SFA Stent System in the treatment of de novo and/or restenotic lesions or occlusions in the Superficial Femoral Artery (SFA) and/or Proximal Popliteal Artery (PPA) in subjects with symptomatic Peripheral Artery Disease (PAD).

NCT ID: NCT00805831 Completed - Atherosclerosis Clinical Trials

Safety and Efficacy of Using HDH Device and Method - a Novel Sutureless Vascular Anastomosis

Start date: October 2008
Phase: N/A
Study type: Interventional

The HDH device is intended for creating sutureless vascular anastomosis in various blood vessels. The HDH device consists of four parts: an elastic tube (graft), docking head (anastomotic device), inversion device (connects the vascular graft to HDH) and measuring device. This study was design in order to evaluate the safety and efficacy of using HDH device and method an innovative anastomotic device for sutureless aortic anastomosis in patient diagnosed with abdominal aneurysm or Aorto-iliac aneurysm.

NCT ID: NCT00804024 Completed - Heart Diseases Clinical Trials

ClearWay™ RX Registry Trial

Start date: August 2008
Phase: N/A
Study type: Observational [Patient Registry]

The primary goal of this registry is to collect data regarding the use of the ClearWay RX Local Therapeutic Infusion Catheter for all indications.

NCT ID: NCT00797056 Completed - Clinical trials for Peripheral Vascular Diseases

Stem Cell Mobilization by G-CSF to Treat Severe Peripheral Artery Disease

STEMPAD
Start date: April 2008
Phase: Phase 0
Study type: Interventional

This study is designed to test the use of G-CSF in peripheral vascular disease. The investigators hypothesize that mobilization of angiogenic cells into the blood by granulocyte colony stimulating factor (G-CSF) may stimulate the formation of new blood vessels and result in a sustained improvement in blood flow in patients with severe peripheral arterial disease.

NCT ID: NCT00796692 Completed - Pulmonary Embolism Clinical Trials

Nadroparin for the Initial Treatment of Pulmonary Thromboembolism

NATSPUTE
Start date: June 2002
Phase: Phase 4
Study type: Interventional

Low-molecular-weight heparin (LWMH) appears to be at least as effective and safe as standard, unfractionated heparin (UFH)for the treatment of patients with deep vein thrombosis(DVT) and may also be so in patients with pulmonary thromboembolism (PTE). Only limited data are available on the evaluation of body weight adjusted LWMH and standard UFH for the initial treatment of PTE in Chinese population. The aim of this study is to determine whether body weight-adjusted, subcutaneous Nadroparin is as effective and safe as UFH for treatment of patients with objectively documented PTE.

NCT ID: NCT00785031 Completed - Clinical trials for Cardiovascular Diseases

Internet Based Vascular Risk Factor Intervention and Self Management Study

IRIS
Start date: October 2008
Phase: N/A
Study type: Interventional

The objective of the study is to evaluate the efficacy and cost-effectiveness of an internet based vascular risk factor program on top of usual care compared to usual care alone for treatment of vascular risk factors in patients at high risk for new vascular events.

NCT ID: NCT00782015 Completed - Hypertension Clinical Trials

Effects of Almonds on Vascular Reactivity in Patients With Coronary Artery Disease

Start date: October 2008
Phase: N/A
Study type: Interventional

This is a study of the effects of 3 oz almonds added daily to a National Cholesterol Education Program Therapeutic Lifestyle Changes (TLC) diet in improving endothelial function in patients with Coronary Artery Disease. The study seeks to determine if these effects are mediated via an increase in Nitric Oxide synthesis and reductions in dyslipidemia and systemic inflammation. Vascular reactivity will be assessed via flow mediated dilation with endothelium-independent and hyperemic flow measured in the right brachial artery by non-invasive 2-dimensional and Doppler ultrasound. Serum will be collected and analyzed for biomarkers of dyslipidemia, inflammation, endothelial function, vascular reactivity and oxidative stress.