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Coronary Artery Disease clinical trials

View clinical trials related to Coronary Artery Disease.

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NCT ID: NCT00165035 Completed - Coronary Disease Clinical Trials

Cobalt Chromium Stent With Antiproliferative for Restenosis II Trial (COSTAR II)

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

The purpose of this study is to evaluate the safety and effectiveness of the investigational stent CoStar™ Paclitaxel-Eluting Coronary Stent- a reservoir based DES system in comparison to a surface coated DES stent (TAXUS™ Express2™ Paclitaxel-Eluting Coronary Stent) in the treatment of single-vessel (one blood vessel) and multi-vessel (two or three blood vessels) coronary artery disease.

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: NCT00163202 Completed - Clinical trials for Hypercholesterolemia

Comparative Atorvastatin Pleiotropic Effects

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

The primary objective of the study is to evaluate the efficacy of atorvastatin 80 mg daily as compared to atorvastatin 10 mg daily in reducing C-reactive protein levels over a 26-week treatment period in subjects with documented coronary artery disease.

NCT ID: NCT00162370 Completed - Clinical trials for Coronary Artery Disease

A Study of Stress Echocardiography in Post-Menopausal Women at Risk for Coronary Disease

Start date: April 2004
Phase: Phase 4
Study type: Interventional

The study is designed to see if stress echocardiography can be used as a screening exam in peri-, or post-menopausal women with a risk of developing of coronary artery disease and experiencing future cardiac events.

NCT ID: NCT00157716 Completed - Myocardial Ischemia Clinical Trials

MEND-CABG (MC-1 to Eliminate Necrosis and Damage in Coronary Artery Bypass Graft Surgery)

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

The purpose of this study is to determine whether MC-1 is effective and safe in reducing cardiovascular and neurological events in patients undergoing high-risk coronary artery bypass surgery

NCT ID: NCT00156845 Completed - Clinical trials for Coronary Artery Disease

Phase 3 Safety and Imaging Study of AI-700 in Patients With Suspected Coronary Artery Disease Undergoing Coronary Angiography

Start date: December 2003
Phase: Phase 3
Study type: Interventional

This study was designed to evaluate the ability of AI-700-enhanced rest-stress echocardiography to detect coronary artery disease (CAD) in patients with suspected ischemic heart disease who are indicated for coronary angiography.

NCT ID: NCT00156793 Completed - Clinical trials for Coronary Artery Disease

Phase 3 Imaging and Safety Study of AI-700 in Patients With Suspected Coronary Artery Disease Undergoing SPECT Imaging

Start date: December 2003
Phase: Phase 3
Study type: Interventional

This study was designed to evaluate the ability of AI-700-enhanced rest-stress echocardiography to detect coronary artery disease (CAD) in patients with suspected ischemic heart disease who are indicated for single-photon emission computed tomography (SPECT) imaging.

NCT ID: NCT00151658 Completed - Clinical trials for Ischaemic Heart Disease

Sirolimus Eluting Stents in Complex Coronary Lesions (SCANDSTENT)

Start date: October 2002
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the clinical and angiographic outcome of implantation of stents eluting or not eluting Sirolimus in patients with complex coronary artery lesions suitable for percutaneous coronary intervention.

NCT ID: NCT00150826 Completed - Clinical trials for Ischemic Heart Disease

QWISE - Study of Quinapril in Women With Chest Pain, Coronary Flow Reserve Limitations and Evidence of Myocardial Ischemia

Start date: May 2000
Phase: Phase 4
Study type: Interventional

INDICATION Microvascular angina. OBJECTIVES To investigate the effect of ACE (angiotensin converting enzyme) inhibition (quinapril) in improving coronary microvascular function. PATIENT POPULATION Women who meet the National Heart, Lung and Blood Institute-sponsored WISE (Women Ischemia Syndrome Evaluation) study criteria of chest discomfort, coronary flow reserve limitations and evidence for myocardial ischemia in the absence of significant coronary artery stenosis. STUDY DESIGN A prospective, randomized, placebo-controlled, comparative trial. TREATMENT Quinapril 80 mg/d versus placebo for four months. PRIMARY EFFICACY PARAMETER(S) Coronary flow reserve (CFR) at Week 16 adjusted for baseline CFR, treatment group assignment, site-specific variables, and site by treatment effects. SECONDARY EFFICACY PARAMETERS Week 16 change in chest discomfort as measured by the Seattle Angina Questionnaire adjusting for baseline values, site, and site by treatment effects. SAFETY PARAMETERS Hematology, blood chemistries, blood pressure and pulse, and frequency and occurrence of adverse events. STATISTICAL RATIONALE AND ANALYSIS A statistical rationale for the number of patients in the study has been provided. Interim analyses are planned after 15 patients have been enrolled in each group. ANTICIPATED TOTAL NUMBER OF PATIENTS 78 (39 per group). ANTICIPATED NUMBER OF PATIENTS AT EACH SITE Approximately 26