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Coronary Disease clinical trials

View clinical trials related to Coronary Disease.

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NCT ID: NCT01589536 Recruiting - Clinical trials for Cardiovascular Events

Social Medical Progression of Coronary Heart Disease With Associated Psychosocial Comorbidity -Interval Rehabilitation.

SINKO
Start date: October 2011
Phase: N/A
Study type: Interventional

The purpose of the study is to verfiy the hypothesis if a short intensive psychocardiological interval-intervention, combined with a structured follow up, decreases the rate of disability retirements caused by psychosocial co-morbidity of patients with coronary heart disease.

NCT ID: NCT01581515 Recruiting - Clinical trials for Coronary Artery Disease

Assessment of Stent Malapposition and Neointimal Coverage on Optical coHerence Tomography at Post-procedure and 3 Months After Platinum Chromium Alloy Of the Element™ Stent Implantation

ANCHOR
Start date: January 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the degree of stent malapposition on an immediate optical coherence tomography (OCT) after nominal stent pressure and at a final post-procedure OCT (ANCHOR-I) and the neointimal coverage on 3-months OCT following the intervention with the randomly assigned two drug-eluting stents (DES), PromusTMElementTM stents versus Xience PRIME® stents.

NCT ID: NCT01567774 Recruiting - Clinical trials for Coronary Artery Disease

Pharmacodynamic Effects of Atorvastatin vs. Rosuvastatin on Platelet Reactivity

PEARL
Start date: April 2012
Phase: Phase 4
Study type: Interventional

Patients with coronary artery disease (CAD) are often treated with dual antiplatelet therapy (DAT), including aspirin and clopidogrel, to prevent from recurrent atherothrombotic events. Levels of platelet reactivity in patients on DAT can be influenced by concomitant treatment with medications that inhibit the CYP3A4 system involved in the activation of clopidogrel. Atorvastatin and simvastatin are metabolized by CYP3A4 [Clin pharmacokinetic 2002; 41: 343-70], whereas the cytochrome P450 mediated metabolism of rosuvastatin appears to be minimal and principally mediated by the 2C9 isoenzyme, with little involvement of CYP3A4 [Clin Ther 2003; 25: 2822-5.]. Previous studies comparing atorvastatin versus rosuvastatin by means of ex vivo platelet function tests have yielded conflicting results.

NCT ID: NCT01563952 Recruiting - Clinical trials for Coronary Artery Disease

Impact of Intravascular Ultrasound(IVUS)-Guided Chronic Total Occlusion Intervention With Drug-eluting Stents

CTO
Start date: October 2010
Phase: Phase 4
Study type: Interventional

Guidance of stenting by IVUS has been proposed as a method to reduce restenosis rates, because lumen and stent dimensions can be accurately determined by intravascular ultrasound (IVUS).

NCT ID: NCT01562730 Recruiting - Clinical trials for Coronary Artery Disease

Myovista iECG for Detecting Ischemic Heart Disease: Comparison With Computed Tomography Coronary Angiography

Start date: April 2012
Phase: Phase 2
Study type: Observational

Study evaluates the new technique MyoVista™ iECG sensitivity and ability to predict myocardial diseases, comparing iECG results with Computed Tomography Coronary Angiography findings

NCT ID: NCT01542086 Recruiting - Chest Pain Clinical Trials

Comparison of the Cost-Effectiveness of Coronary CT Angiography Versus Myocardial SPECT in Patients With Intermediate Risk of Coronary Heart Disease

CARE-CCTA
Start date: September 2011
Phase: N/A
Study type: Interventional

The investigators aim to compare the cost-effectiveness of CCTA and myocardial SPECT in patients with intermediate pre-test probability of CHD. To this end, patients with intermediate pre-test probability of CHD will be randomized 1:1 to either CCTA and myocardial SPECT. The patients will be analyzed for cost and also, for outcome.

NCT ID: NCT01542073 Recruiting - Clinical trials for Coronary Artery Disease

68Ga-BNOTA-PRGD2 PET/CT in Evaluation of Myocardial Infarction

GRGDMI
Start date: February 2012
Phase: Early Phase 1
Study type: Interventional

This is an open-label PET/CT (positron emission tomography/computed tomography) study to investigate the diagnostic performance of 68Ga-BNOTA-PRGD2 in evaluation of myocardial infarction. A single dose of nearly 111 MBq 68Ga-BNOTA-PRGD2 ( ≤ 40 µg BNOTA-PRGD2) will be intravenously injected into myocardial infarction patients. Visual and semiquantitative method will be used to assess the 68Ga-BNOTA-PRGD2 PET/CT cardiac images and compared to the 99mTc-MIBI SPECT myocardial perfusion images and the 18F-FDG metabolism images.

NCT ID: NCT01535625 Recruiting - Clinical trials for Coronary Artery Disease

Safety and Effectiveness of the Coronary Momo Stent

Start date: February 2012
Phase: Phase 4
Study type: Interventional

This study evaluates the safety and effectiveness of the Momo Cobalt Chromium stent system for the treatment of single de novo lesions in a native coronary artery. The stent is coated with diamond-like carbon to decrease the risk of acute and late stent thrombosis, to increase the resistance towards corrosion and to significantly improve endothelialisation through the inhibition of elution of metallic ions.

NCT ID: NCT01531231 Recruiting - Clinical trials for Coronary Artery Disease

Typical Daily Experiences, Ischemia and Repolarization in Coronary Artery Disease

Start date: January 2012
Phase: N/A
Study type: Observational

The purpose of this study is to examine the role of every day experiences as they relate to coronary artery disease (CAD).

NCT ID: NCT01508663 Recruiting - Clinical trials for Coronary Artery Disease

The Beneficial Role of Percutaneous Coronary Intervention Over Optimal Medical Therapy in Elderly Patients With Coronary Artery Disease

BRAVE
Start date: August 2010
Phase: Phase 4
Study type: Interventional

The primary purpose of this study is to determine whether PCI added to OMT could be superior over OMT alone in the prevention of late adverse cardiac and cerebro-vascular events in elderly patients with coronary artery disease (CAD) during the additional 12 months.