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Coronary Artery Disease clinical trials

View clinical trials related to Coronary Artery Disease.

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NCT ID: NCT00789243 Completed - Clinical trials for Ischaemic Heart Diseases

The Effect of Ischaemic-Reperfusion and Ischaemic Preconditioning on the Endogenous Fibrinolysis in Man

Start date: November 2008
Phase: N/A
Study type: Interventional

Heart attacks are usually caused by a blood clot blocking an artery supplying blood to the heart. Current treatments are designed at relieving this blockage as quickly as possible to minimise damage to the heart muscle. However in restoring the supply of blood local damage known as "ischaemia-reperfusion injury" may occur. The aim of this study is to assess how clot forming and clot dissolving pathways are affected during this process, and examine the role of a natural inflammatory hormone, bradykinin. This will help us to understand the mechanism by which ischaemia-reperfusion injury may occur and to devise new treatments for heart attacks.

NCT ID: NCT00788242 Completed - Heart Failure Clinical Trials

The Effect of Glucose-Insulin-Potassium Infusion in Patients Undergoing Cardiac Surgery

Start date: January 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the cardioprotective effects of a short term infusion of glucose-insulin-potassium (GIK) during heart surgery.

NCT ID: NCT00783302 Completed - Clinical trials for Coronary Artery Disease (CAD)

Study in Subjects Suspected of Having CAD Undergoing VISIPAQUE-enhanced CCTA as Part of Their Routine Medical Care

Start date: September 2008
Phase: N/A
Study type: Observational

To assess prognostic value of CCTA examination in subjects who undergo CCTA as part of their medical care when compared to a standard of truth, i.e. subject outcomes during each follow-up period.

NCT ID: NCT00782015 Completed - Hypertension Clinical Trials

Effects of Almonds on Vascular Reactivity in Patients With Coronary Artery Disease

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

This is a study of the effects of 3 oz almonds added daily to a National Cholesterol Education Program Therapeutic Lifestyle Changes (TLC) diet in improving endothelial function in patients with Coronary Artery Disease. The study seeks to determine if these effects are mediated via an increase in Nitric Oxide synthesis and reductions in dyslipidemia and systemic inflammation. Vascular reactivity will be assessed via flow mediated dilation with endothelium-independent and hyperemic flow measured in the right brachial artery by non-invasive 2-dimensional and Doppler ultrasound. Serum will be collected and analyzed for biomarkers of dyslipidemia, inflammation, endothelial function, vascular reactivity and oxidative stress.

NCT ID: NCT00777166 Completed - Myocardial Ischemia Clinical Trials

Cardiac Effects of Oxytocin Administrated During Cesarean Section, Signs of Myocardial Ischemia

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

Oxytocin has cardio vascular effects as hypotension, tachycardia and possibly coronary spasm. The uterotonic effect of the drug is used during cesarean section, to minimize blood loss.ECG changes suggestive of cardiac ischemia (ST depression) has been showed in previous studies of patients undergoing cesarean section i regional anaesthesia. The effect of oxytocin on this outcome has not been investigated to any extent. In the current study, we tested the hypothesis that there was no difference in occurrence of ECG changes (ST segment depression) between two doses of oxytocin. Participants were randomized to receive either 5 or 10 units of oxytocin in a double blinded fashion. Main outcome measure is occurrence of significant ST depression on ECG. Secondary outcome measures are mean arterial pressure, heart rate, blood loss, symptoms as chest pain, shortness of breath and feeling of heaviness on the chest.

NCT ID: NCT00776828 Completed - Clinical trials for Coronary Artery Disease

The Efficacy of CILostazol ON Ischemic Complications After DES Implantation

CILON-T
Start date: November 2006
Phase: Phase 4
Study type: Interventional

Objectives : - To evaluate the influence of concomitant use of cilostazol with aspirin and clopidogrel on the composite cardiovascular adverse outcomes (cardiac death, myocardial infarction, nonhemorrhagic stroke, target lesion revascularization) after drug-eluting stent implantation Study Design : Prospective, open label, two arm, randomized multicenter trial to test the superiority of cilostazol group compared with the control group. Patients will be randomized according to the use of cilostazol Patient Enrollment: 960 patients enrolled at 5 centers in Korea Patient Follow-up : Clinical follow-up will occur at 1, 3 and 6 months. Angiographic follow-up will be recommended to all patient at 6 months after index procedure. Primary Endpoint - Composite of adverse cardiovascular/cerebrovascular outcomes (cardiac death, myocardial infarction, nonhemorrhagic stroke, target lesion revascularization) within 6 months Secondary Endpoint - All cause of death, stent thrombosis, and each component of primary endpoint at six months - PRU level measured at discharge after the index procedure and after six months Safety Endpoint - Bleeding complications according to TIMI criteria - The incidence of drug discontinuation - Heart rate

NCT ID: NCT00776204 Completed - Clinical trials for Coronary Artery Disease

The Optical Coherence Tomography Drug Eluting Stent Investigation

OCTDESI
Start date: May 2008
Phase: N/A
Study type: Interventional

The objective of this study is to evaluate the completeness of struts coverage and vessel wall response to the new generation JACTAX drug-eluting stent vs Taxus stent in de novo coronary artery lesions at 6 months post index procedure. To investigate the completeness of the coverage as well as the number of uncovered stent struts per section, high resolution (~ 10-15 µm axial) intracoronary Optical Coherence Tomography (OCT) will be used.

NCT ID: NCT00774865 Completed - Clinical trials for Coronary Artery Disease

Long Term Follow-up of Robotic Assisted Surgical Revascularization

ZEUSFUPCTA
Start date: June 2008
Phase:
Study type: Observational

The objectives of the 2-year study are two-fold: 1. To determine the 5-7 year patency rate (rate of open bypass grafts) of the LITA graft of patients who have already had robotically-assisted CABG surgery using CTA and MPS-MIBI 2. To determine patient quality of life at 5-7 years after robotically-assisted CABG surgery

NCT ID: NCT00773006 Completed - Clinical trials for Coronary Artery Disease

Canadian Anticoagulant Percutaneous Coronary Intervention Registry

CAPCIR
Start date: February 2008
Phase: N/A
Study type: Observational

Advances in mechanical intervention (PCI) and anticoagulation therapy have been the cornerstone of treatment of patients with coronary artery disease. However, the large diversity of approaches to anticoagulation during PCI introduces gaps in knowledge regarding management of cardiac patients. As such, we have initiated a national PCI registry to elucidate anticoagulant choice, dosing strategies, case selection dynamics, and clinical outcomes in the Canadian health care environment.

NCT ID: NCT00771004 Completed - Clinical trials for Coronary Artery Disease

Efficacy of Pioglitazone on Myocardial Function in Patients Undergoing Coronary Stent Implantation.

Start date: August 2006
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the effects of pioglitazone, once daily (QD), on heart functioning before, during and after stent implantation.