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Coronary Artery Disease clinical trials

View clinical trials related to Coronary Artery Disease.

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NCT ID: NCT00914199 Active, not recruiting - Clinical trials for Coronary Artery Disease

The Nordic Bifurcation Study III

BIF III
Start date: April 2, 2007
Phase: N/A
Study type: Interventional

Should we, or should we not, perform dilatation of the side branch through the main vessel stent, if there is acceptable blood flow in the side branch?

NCT ID: NCT00911339 Terminated - Clinical trials for Stable Coronary Artery Disease

Mobilization of Endothelial Progenitor Cells Induced by Atorvastatin in Patients With Stable Coronary Artery Disease Treated With Anti-CD 34 Antibodies Coated Stents

Start date: January 2009
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the extent of the mobilization of endothelial progenitor cells induced by low versus high dose atorvastatin after 4 weeks of treatment, in patients treated with anti-CD 34 antibodies coated stent.

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: NCT00910299 Terminated - Clinical trials for Coronary Artery Disease (CAD)

Testing Platelet Reactivity In Patients Undergoing Elective Stent Placement on Clopidogrel to Guide Alternative Therapy With Prasugrel (TRIGGER-PCI)

TRIGGER-PCI
Start date: July 2009
Phase: Phase 2
Study type: Interventional

To determine the efficacy of prasugrel versus clopidogrel for the reduction of adverse cardiovascular outcomes in patients with high platelet reactivity on clopidogrel after successful implantation of coronary drug-eluting stents. To determine the adverse event profile of prasugrel in patients with high platelet reactivity on clopidogrel after implantation of coronary drug-eluting stents. To determine the effect of prasugrel on inhibition of platelet activation in patients with high platelet reactivity on clopidogrel.

NCT ID: NCT00908518 Not yet recruiting - Clinical trials for Cognitive Dysfunction

The Difference in Postoperative Cognitive Dysfunction and Myocardial Ischemia Between Propofol and Isoflurane

POCD
Start date: June 2009
Phase: N/A
Study type: Observational

The progressive aging of the general population cause increase in number of extensive and long surgeries in older patients. Age is a risk factor for perioperative myocardial ischemia and Postoperative Cognitive Dysfunction (POCD) The suggested study will deal with the above-mentioned complication in patients older then 65 years undergoing major non-cardiac surgeries. It has been shown that Isoflurane and sevoflurane may have a cardio-protective effect after cardiac surgery involving cardio-pulmonary bypass, and it was recommended that isoflurane should be used in these cases. A question was raised but haven't been answered yet, whether this cardio-protective effect exists also in non-cardiac major surgery. The aim of this study is to evaluate whether there is a difference in the occurrence of postoperative cognitive dysfunction and perioperative myocardial ischemia between total intravenous anesthesia using propofol and isoflurane based anesthesia.

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: NCT00907764 Terminated - Clinical trials for Coronary Artery Disease

Stress Echocardiography Study With Regadenoson

Start date: April 2009
Phase: Phase 2
Study type: Interventional

Regadenoson is approved in the US under the brand name Lexiscan for myocardial perfusion imaging. This study will test whether regadenoson is an appropriate stress agent for stress echocardiography.

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.

NCT ID: NCT00905853 Completed - Clinical trials for Recurrent Ventricular Tachycardia

Ventricular Tachycardia (VT) Ablation or Escalated Drug Therapy

VANISH
Start date: May 2009
Phase: Phase 4
Study type: Interventional

This study will compare aggressive antiarrhythmic therapy to catheter ablation for ventricular tachycardia in patients who have suffered prior myocardial infarction. The purpose of this study is to evaluate the optimal management of patients presenting with recurrent VT and receiving ICD therapy in spite of first-line antiarrhythmic drug therapy. The hypothesis is catheter ablation is superior to aggressive antiarrhythmic drug therapy for recurrent VT.