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Coronary Artery Disease clinical trials

View clinical trials related to Coronary Artery Disease.

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NCT ID: NCT01107925 Completed - Clinical trials for Coronary Artery Disease

Comparison of Prasugrel and Clopidogrel in Low Body Weight Versus Higher Body Weight With Coronary Artery Disease

FEATHER
Start date: March 2010
Phase: Phase 1
Study type: Interventional

The 5-milligram (mg) dose of prasugrel in low body weight (LBW) patients with coronary artery disease produces a pharmacodynamic response within the same therapeutic range as 10-mg dose in higher body weight (HBW) patients.

NCT ID: NCT01107912 Completed - Clinical trials for Coronary Artery Disease

Comparison of Prasugrel and Clopidogrel in Very Elderly and Non-Elderly Patients With Stable Coronary Artery Disease

GENERATIONS
Start date: March 2010
Phase: Phase 1
Study type: Interventional

The 5-milligram (mg) maintenance dose (MD) of prasugrel in very elderly patients with coronary artery disease produces a pharmacodynamic response within the same therapeutic range as 10-mg MD in non-elderly patients.

NCT ID: NCT01106534 Completed - Clinical trials for Coronary Artery Disease

XIENCE V® USA Dual Antiplatelet Therapy (DAPT) Cohort

XVU-AV DAPT
Start date: August 2009
Phase: Phase 4
Study type: Interventional

XIENCE V USA is a prospective, multi-center, multi-cohort postapproval study. The objectives of this study are - To evaluate XIENCE V EECSS continued safety and effectiveness during commercial use in real world settings, and - To support the Food and Drug Administration (FDA) dual antiplatelet therapy (DAPT) initiative. This initiative is designed to evaluate the composite of all death, myocardial infarction (MI) and stroke (MACCE) and the survival of patients that are free from Academic Research Consortium (ARC) definite or probable stent thrombosis (ST) and that have been treated with drug eluting stents (DES) and extended dual antiplatelet therapy.

NCT ID: NCT01102439 Completed - Clinical trials for Coronary Artery Disease

Clopidogrel/Aspirin Interaction Study

INTERACTION
Start date: April 2010
Phase: Phase 4
Study type: Interventional

This study will explore the effect of different doses of aspirin on the effects of double-dose or standard dose clopidogrel.

NCT ID: NCT01100385 Completed - Stroke Clinical Trials

TomVasc - Vascular Effects of Tomato Extract

TomVasc
Start date: February 2010
Phase: N/A
Study type: Interventional

Does tomato extract improve blood vessel function in healthy people and people with cardiovascular disease? Atherosclerosis ('furring' of the arteries) affects the functioning of blood vessels, narrowing and eventually blocking them, causing conditions like heart attack and stroke. The Mediterranean diet, which is rich in tomatoes and tomato-based products, has been shown to be associated with a reduced risk of blood vessel damage. In this double blind, placebo-controlled randomised study, the investigators will investigate whether a food supplement containing a standardised extract of tomato improves blood vessel function in both healthy people (aged 40-80), and people with a history of cardiovascular disease. The food supplement is on sale to the public, and the investigators are testing the standard dose. Approximately 72 people will take part at the Clinical Pharmacology Unit at the ACCI Building, Cambridge University Hospitals NHS Trust. After they have passed screening tests, participants will be allocated by chance to receive either the tomato extract product (Ateronon), or a matching placebo (a dummy capsule with no active ingredients), which they will take once a day for 8 weeks. At the beginning and end of the treatment period, the investigators will test blood vessel stiffness using an ECG machine and external probe. The investigators will also measure forearm blood flow, which involves infusing 3 separate agents that affect how the lining of the blood vessel wall works, and helps to assess whether this is affected by the study treatment. Blood tests will also be used to look at how the food supplement is working and its effects on cholesterol and markers of inflammation. Including the screening period, and a follow-up telephone call two weeks after the end of treatment, participants will be in the study for 14 weeks.

NCT ID: NCT01098591 Completed - Clinical trials for Ischemic Heart Disease

Meta-Analysis of Cell-based CaRdiac stUdiEs: ACCRUE

ACCRUE
Start date: November 2007
Phase:
Study type: Observational

Numerous human cardiac stem cell studies have been published, including relatively small number of patients. Meta-analysis of randomized trials have reported safety and a 3-6% increase in global left ventricular performance after intracoronary stem cell therapy in patients with acute myocardial infarction. Since most of the studies used different type of stem cells, delivery modes, and patient population, the results are heterogenous, therefore the comparison of the results is biased regarding generalizable conclusions about the effect of treatment. The present comparative meta-analysis is based on individual patient data, and gathers and pools the raw data, and analyzes the clinical outcome, safety and efficacy of the cardiac stem cell therapy.

NCT ID: NCT01097434 Completed - Clinical trials for Coronary Heart Disease

Test Safety of Biodegradable and Permanent Limus-Eluting Stents Assessed by Optical Coherence Tomography

TEST-6-OCT
Start date: April 2010
Phase: Phase 4
Study type: Interventional

The objective of the study is to assess the superiority of the biodegradable polymer based limus-eluting stent (Nobori®) compared with the permanent polymer based everolimus-eluting stent (XIENCE V®) regarding absolute percentage of uncovered stent strut segments.

NCT ID: NCT01094275 Completed - Clinical trials for Coronary Artery Disease

Role of CYP2C19 Polymorphism in the Drug Interaction Between Clopidogrel and Omeprazole

Start date: January 2010
Phase: N/A
Study type: Observational [Patient Registry]

Clopidogrel, an inhibitor of ADP induced platelet aggregation and activation, is one of the most commonly used drugs in patients with cardiovascular disease. The specific aim of the proposed study is to determine whether the interaction between proton-pump inhibitors (PPIs) and clopidogrel is dependent on CYP2C19 haplotype.

NCT ID: NCT01093391 Completed - Clinical trials for Coronary Artery Disease

A Trial of Bare Metal Stent - Cobalt Chromium Versus Stent Coating With Sirolimus

INSPIRON
Start date: November 2010
Phase: Phase 3
Study type: Interventional

The objective of this study is to evaluate the security issues and efficacy of coronary stenting Cobalt Chrome covered with sirolimus-eluting Cobalt Chrome platform in patients with coronary artery lesion.

NCT ID: NCT01092793 Completed - Clinical trials for Stable Atherosclerotic Coronary Disease

Effect of Superba Krill on Inflammation in Patients With Coronary Artery Disease

Start date: February 2010
Phase: N/A
Study type: Interventional

Atherosclerotic coronary heart disease is a condition thought to involve low-grade inflammation. Several reports, clinical and epidemiological, have demonstrated that intake of fish oil may be beneficial in attenuating the inflammatory process. Still, however, there are lacking data in respect to whether differences in composition of various marine oils may influence the inflammatory status differently. The hypothesis of the current study is that extract from the antarctic krill (Euphausia superba) is better than traditional fish oils when compared head-to-head with balanced composition of omega 3 content on inflammatory status.