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Coronary Artery Disease clinical trials

View clinical trials related to Coronary Artery Disease.

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NCT ID: NCT00919373 Completed - Clinical trials for Coronary Artery Disease

Substrate Modification in Stable Ventricular Tachycardia in Addition to Implantable Cardioverter Defibrillator (ICD) Therapy

VTACH
Start date: July 2002
Phase: N/A
Study type: Interventional

The main objective of this study is to compare the time from randomization to the first recurrence of any ventricular tachycardia (VT) in patients undergoing VT ablation (for stable VTs) and substrate ablation (for unstable VTs) after an initial episode of stable VT and patients not undergoing ablation, with both groups under the protection of an ICD.

NCT ID: NCT00918372 Completed - Clinical trials for Coronary Artery Disease

Coronary Artery Disease (CAD) in Women Marathon Runners

Start date: May 2009
Phase: N/A
Study type: Observational

The aim of this study is to determine the effects of extreme fitness in women. The incidence of coronary artery disease observed via multislice computed tomography (MSCT) angiogram will be compared with age and risk-matched controls from both sedentary and fitness activity groups who have never been significant runners. Life style, training volume and risk factors will be assessed.

NCT ID: NCT00917930 Completed - Clinical trials for Coronary Artery Disease

Evaluation Rehabilitation on Glycometabolic State in Non-Diabetic Coronary Artery Disease (CAD) Patients

Start date: January 2006
Phase: Phase 4
Study type: Observational

The purpose of this study is to evaluate the effects of an intensive Cardiac rehabilitation program on glucose metabolism of non-diabetic coronary artery disease patients.

NCT ID: NCT00917124 Completed - Clinical trials for Coronary Artery Disease

Cerebral Oximetry and Neurocognitive Functions in Cardiosurgical Patients

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

It is previously reported that the cerebral oxygen desaturation during cardiac surgery is associated with an increased incidence of cognitive impairment. The aim of this study is to determine whether intraoperative monitoring and predetermined interventions protocol to improve cerebral oxygenation during coronary artery bypass surgery provides benefits in neurocognitive functions.

NCT ID: NCT00916370 Completed - Clinical trials for Coronary Artery Disease

SPIRIT PRIME Clinical Trial

SPIRIT PRIME
Start date: June 2009
Phase: Phase 3
Study type: Interventional

To evaluate the safety and effectiveness of the XIENCE PRIME and XIENCE PRIME Long Lesion (LL) Everolimus Eluting Coronary Stent System (EECSS) in improving coronary luminal diameter in subjects with symptomatic heart disease due to a maximum of two de novo native coronary artery lesions, each in a different epicardial vessel.

NCT ID: NCT00914368 Completed - Clinical trials for Coronary Artery Disease

Tailoring Of Platelet Inhibition to Avoid Stent Thrombosis

TOPAS-1
Start date: January 2009
Phase: Phase 2
Study type: Interventional

The primary objective of this study is to establish a cut off level of platelet inhibition that separates patients with or without previous stent occlusion with acute clinical onset while on aspirin and clopidogrel treatment within 6 months after coronary stenting for coronary artery disease.

NCT ID: NCT00910481 Completed - Clinical trials for Coronary Artery Disease

Balloon Pump Assisted Coronary Intervention Study

BCIS-1
Start date: December 2005
Phase: N/A
Study type: Interventional

This study will test the hypothesis that elective use of the Intra-Aortic Balloon Pump (IABP) in patients undergoing high-risk Percutaneous Coronary Intervention (PCI) will reduce the rate of in-hospital major adverse cardiac and cerebrovascular events compared to patients who are managed without planned insertion of IABP.

NCT ID: NCT00907998 Completed - Clinical trials for Coronary Heart Disease

Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of APL180

Start date: June 2009
Phase: Phase 1
Study type: Interventional

The design of this study will enable an extensive evaluation of safety, tolerability, and PK-PD relationship following 4 weeks of dosing in patients with Coronary heart Disease

NCT ID: NCT00907855 Completed - Clinical trials for Ischemic Heart Disease

Using Duke Activity Status Index (DASI) to Select Optimal Cardiac Stress Tests

DASI-08-713
Start date: April 2009
Phase: N/A
Study type: Observational

Cardiac stress testing with functional nuclear imaging is an invaluable technique in the diagnostic and prognostic evaluation of patients with known or suspected ischemic heart disease. Selection of the appropriate type of nuclear stress test: exercise stress Myocardial Perfusion Imaging (MPI) versus pharmacologic stress MPI is crucial for not only diagnostic accuracy and prognostic evaluation, but also for sound clinical decisions and resource utilization. The Duke Activity Status Index (DASI) is a 12-item questionnaire that utilized self-reported physical work capacity to estimate peak metabolic equivalents (METs) and has been shown to be a valid measurement of functional capacity. The investigators hypothesized that the DASI may be the screening tool that evaluates functional capacity and guides selection of the optimal stress MPI study.

NCT ID: NCT00907439 Completed - Clinical trials for Coronary Artery Disease

Study of the Effect of Inhaled Anesthetics on Diastolic Heart Function Using a Doppler-derived Efficiency Index

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

The purpose of this study is to determine the effect of inhaled anesthetic drugs upon diastolic heart function (heart suction and filling performance) in patients who are undergoing coronary bypass surgery.