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Coronary Heart Disease clinical trials

View clinical trials related to Coronary Heart Disease.

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NCT ID: NCT00222261 Completed - Atherosclerosis Clinical Trials

Aspirin Non-responsiveness and Clopidogrel Endpoint Trial.

ASCET
Start date: April 2003
Phase: Phase 4
Study type: Interventional

In the ASCET study, 1000 patients with documented coronary heart disease will be randomized to either continued treatment with aspirin 160 mg/d or change to clopidogrel 75mg/d. Clinical endpoints will be recorded for at least 2 years and related to the initial aspirin response, assessed by the PFA-100® method, to investigate whether aspirin non-responders have higher composite event rate than responders or whether Clopidogrel treatment in patients non-responsive to aspirin will reduce their risk of future clinical events. The clinical events are the composite of unstable angina, myocardial infarction, stroke or death.

NCT ID: NCT00202904 Completed - Clinical trials for Hypercholesterolemia

Effectiveness and Safety of Ezetimibe Added to Atorvastatin in Patients With High Cholesterol and Coronary Heart Disease (Study P03740)

Start date: May 2005
Phase: Phase 4
Study type: Interventional

This is a multicenter, randomized, parallel group, placebo controlled study designed to evaluate the efficacy, safety, and tolerability of ezetimibe added to ongoing atorvastatin therapy compared with ongoing atorvastatin treatment alone. This study will involve subjects with primary hypercholesterolemia and coronary heart disease (CHD) who are currently being treated with atorvastatin and who would benefit from additional reduction in low-density lipoprotein cholesterol (LDL-C).

NCT ID: NCT00185042 Completed - Clinical trials for Coronary Heart Disease

Efficacy and Safety of the ACAT Inhibitor CS-505 (Pactimibe) for Reducing the Progression of Coronary Artery Disease

Start date: November 2002
Phase: Phase 2
Study type: Interventional

The purpose of this study is to learn if CS-505 is safe and effective for slowing down or possibly reversing the buildup of tissue, cells and fatty deposits (plaque) in the blood vessels of the heart (coronary artery atherosclerosis).

NCT ID: NCT00164658 Completed - Breast Cancer Clinical Trials

Evaluating Tools for Health Promotion and Disease Prevention

Start date: September 2005
Phase: Phase 1
Study type: Interventional

The study will evaluate the effect of familial risk assessment and prevention prompts tailored to familial risk on health behaviors and use of preventive services among adults who are members of primary care practices in the U.S.

NCT ID: NCT00163683 Completed - Type 2 Diabetes Clinical Trials

Effects of a Mediterranean Style Diet on Vascular Health in Type 2 Diabetes

Start date: January 2003
Phase: N/A
Study type: Interventional

In this study we will compare the effects of a Mediterranean diet, high in fruit and vegetables with the more conventional diet recommended for diabetes therapy (a high carbohydrate, low fat diet) on glycaemic and lipid control and on markers of inflammation, in people with newly diagnosed Type 2 diabetes. The hypothesis is that, over a six-month intervention period, a HVM diet will be more effective than a conventional HCLF diet in improving glycaemic and lipid control, and in reducing markers of vascular inflammation in people with Type 2 diabetes.

NCT ID: NCT00146315 Completed - Clinical trials for Coronary Heart Disease

ESCAP: Supervised Exercise for Patients With Coronary Heart Disease in the Primary Care Setting

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

In Spain, family physician are currently recommended to prescribe an unsupervised walking program to their coronary heart disease (CHD) patients as a part of their cardiac rehabilitation program. However, there are a few family physicians who provide their CHD patients with supervised exercise (30 minutes of pedaling on an stationary bicycle at 60-85% of the peak heart rate (HR) attained at the maximal or symptom limited treadmill test, 3 times a week) at their primary care health centers, thinking that these patients improve their functional capacity, quality of life, and the control of cardiovascular risk factors, more than walking because they can not achieve the ideal exercise intensity for maximal benefits by walking. This study has been designed to investigate if CHD patients get more health benefits with the supervised exercise program at the health center than with the unsupervised walking program.

NCT ID: NCT00139958 Completed - HIV Infection Clinical Trials

Prognosis of Acute Coronary Syndrome in HIV-infected Patients

Start date: November 2003
Phase: Phase 4
Study type: Observational

Objectives: Evaluate differences for mortality, morbidity and the cardiovascular risk factors between HIV and non-HIV patients with an acute coronary syndromes (ACS) after a 3-years follow up.

NCT ID: NCT00134940 Completed - Clinical trials for Coronary Heart Disease

Post-marketing Study to Collect Safety Data in Heart Transplant Patients Receiving Everolimus

Start date: January 2005
Phase: Phase 4
Study type: Observational

The purpose of this observational protocol is to evaluate the use of everolimus in routine clinical practice for heart transplants. Primary outcome measures: incidence of acute rejection episodes Secondary outcomes: safety

NCT ID: NCT00130871 Completed - Clinical trials for Coronary Heart Disease

Levosimendan Pretreatment for Weaning Patients From Cardio-Pulmonary Bypass

Start date: January 2004
Phase: Phase 2
Study type: Interventional

The study evaluates the efficacy of intravenous levosimendan treatment started during a coronary artery bypass operation to wean patients from a heart lung machine.

NCT ID: NCT00127751 Completed - Stroke Clinical Trials

Heart Disease on the Mend

Start date: May 2000
Phase: Phase 2
Study type: Interventional

The primary objective of this study was to evaluate the effectiveness of a multifactor cardiovascular disease (CVD) risk reduction program using team case management in high risk patients who have low family incomes and limited access to medical care. Patients were randomized to case management (99) or usual care (49) with baseline, 6-month and 12-month evaluations of CVD risk factors, clinical status and quality of life.