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Atherosclerosis clinical trials

View clinical trials related to Atherosclerosis.

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NCT ID: NCT00784264 Completed - Atherosclerosis Clinical Trials

A Study on Intima Media Thickness (IMT) in Middle-aged Subjects

IMT
Start date: October 2008
Phase: N/A
Study type: Observational

This is an observational study to measure the thickness of artery walls in the neck (intima media thickness IMT) by ultrasound examination in middle-aged subjects with central obesity. The purpose of this study is to obtain local data how common asymptomatic atherosclerosis is, and to investigate the association between Cardiovascular Disease risk factors and intima media thickness (IMT) in the Hong Kong population. Results from this study may enhance the public awareness of asymptomatic atherosclerosis and understand its role in the development of Cardiovascular Disease in Hong Kong.

NCT ID: NCT00783796 Terminated - Clinical trials for Coronary Artery Disease

SPIRIT Small Vessel Registry

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

To evaluate the safety and effectiveness of the 2.25 mm XIENCE V® Everolimus Eluting Coronary Stent System (XIENCE V® EECSS) in improving coronary luminal diameter in subjects with ischemic heart disease due to a maximum of two de novo native coronary artery lesions in small vessels, each in a different epicardial vessel.

NCT ID: NCT00783042 Completed - Atherosclerosis Clinical Trials

Exploratory Study of Coronary Flow Reserve Measurements, a Non-Invasive Method for Coronary Function Measurements

Start date: October 2008
Phase: Phase 0
Study type: Interventional

The aim of this study is to investigate whether the non-invasive ultrasound method for assessment of coronary blood flow, transthoracic Doppler echocardiography-coronary flow reserve (TTDE-CFR), can be used to measure drug effects.

NCT ID: NCT00776477 Recruiting - Atherosclerosis Clinical Trials

The Clopidogrel and Aspirin After Surgery for Coronary Artery Disease

Start date: December 2007
Phase: Phase 3
Study type: Interventional

Clopidogrel is a antiplatelet agent and is effective at reducing intimal hyperplasia in animal models of thrombosis.Several large clinical trials have demonstrated that clopidogrel with aspirin can reduce ischemic events and mortality in patients with atherosclerotic disease,therefore the combination of two antiplatelets might be useful to prevent patients received coronary artery bypass graft surgery from Saphenous vein graft disease. the aim of this study is to estimate the safety and efficacy of clopidogrel and aspirin therapy versus aspirin alone in patients after CABG.

NCT ID: NCT00768274 Completed - Clinical trials for Cardiovascular Disease

Safety, Pharmacokinetic Study of RVX000222 in Healthy Subjects and Subjects With Low HDL Cholesterol

Start date: September 2008
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to investigate an oral formulation of RVX000222 for safety, pharmacokinetic and efficacy in healthy subjects.

NCT ID: NCT00767663 Completed - Atherosclerosis Clinical Trials

Persantin Preceding Elective PCI

P3
Start date: October 2008
Phase: Phase 4
Study type: Interventional

In this study the investigators will investigate whether a short pretreatment (3-7 days) with dipyridamole 200mg twice daily will protect patients against myocardial injury sustained during an elective dotter operation of the coronary arteries (PCI). The investigators hypothesize that dipyridamole can reduce myocardial injury sustained during elective PCI.

NCT ID: NCT00766896 Completed - Stroke Clinical Trials

Platelet Hyperreactivity to Aspirin and Stroke

PLARAS
Start date: July 2009
Phase: Phase 4
Study type: Interventional

STUDY QUESTIONS - What is the real prevalence of platelet "resistance" to aspirin during the acute phase of stroke and after 3 months, and 1 year, as measured using different platelet function tests? - Do all methods measure similar levels of resistance, or are some methods more sensitive than others? - Does this resistance result in a worse clinical prognosis? Is this result independent of other variables? OBJECTIVES 1. Hospital Phase (Acute Stroke) - Determination, using various methods, of the prevalence of platelet hyperreactivity in patients treated with aspirin to treat ischemic stroke (acute phase) - Comparison of different assessment methods and identification of the most accurate of these - Identification of variables that correlate with platelet hyperreactivity 2. Follow-up Phase - Correlation between platelet hyperreactivity and important clinical outcomes at 12, 24, and 36 months - Correlation between platelet hyperreactivity and death or dependency at hospital discharge, at 3, 12, 24, and 36 months (Modified Rankin Scale) - Correlation between platelet hyperreactivity and recurrent stroke of any type - Correlation between different methods for evaluating platelet functions and identification of the most accurate method - Analysis of hyperreactivity over time THE STUDY - The study will include 200 consecutive patients seen in the emergency department of a large, urban hospital (1500 inpatient beds) and diagnosed with stroke in the acute phase; these patients will be treated with aspirin for an undetermined period - The investigators will not include patients who require full anticoagulation treatment, regardless of the cause - Importantly, the analysis of primary and secondary outcomes will be carried out after blinding the examiner to the results of the platelet aggregation tests PLATELET TESTS - Whole Blood Aggregometer, ChronoLog - VerifyNow, Accumetrics - PFA-100, Siemens - Plateletworks, Helena - Impact-R, Diamed - Serum thromboxane B2

NCT ID: NCT00765310 Active, not recruiting - Atherosclerosis Clinical Trials

Lipoic Acid and Prevention of Heart Disease

Start date: April 2009
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 such as body weight and high blood cholesterol levels in overweight or obese participants.

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: NCT00764010 Completed - Atherosclerosis Clinical Trials

Diet and Omega-3 Intervention Trial on Atherosclerosis

DOIT
Start date: May 1997
Phase: Phase 3
Study type: Interventional

The study was actuated to evaluate the effects of a 3-year intervention with diet and/or very long chain omega-3 (VLC n-3 PUFA), in a randomized 2x2 factorial design on the progression of atherosclerosis in a high risk population. A total of 563 elderly men were included and randomized to receive usual care and VLC n-3 placebo capsules (control group), dietary advice and VLC n-3 placebo capsules, usual care and VLC n-3 capsules, and finally both VLC n-3 capsules and dietary advice. The evaluation of atherosclerosis were i) ultrasound measurement of carotid intima media thickening ii) pulse wave propagation time iii) circulating biomarkers of atherosclerosis.