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Myocardial Ischemia clinical trials

View clinical trials related to Myocardial Ischemia.

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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: 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: NCT00905294 Terminated - Clinical trials for Coronary Artery Disease

Study of ADAMTS-13 Activity, Von Willebrand Factor and Platelet-Monocyte Aggregation in Coronary Artery Disease

ADVANCE-PCI
Start date: August 2009
Phase: N/A
Study type: Observational

The purpose of this research is to determine the relationship between proteins and enzymes in the blood and how they work with platelets to form blood clots in patients with coronary artery disease. The investigators hypothesize that the relationship between these factors could potentially be useful in identifying patients at higher risk for heart attacks.

NCT ID: NCT00893984 Terminated - Clinical trials for Coronary Artery Disease

Alternative in Beta Blocker Intolerance: The ABBI Trial

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

In this study the investigators will assess the tolerance of Nebivolol (Bystolic) in cardiovascular patients who are not able to tolerate conventional beta blockers. A side effect profile will be tracked and compared with previous beta blocker use. The investigators hypothesize that Bystolic will be tolerated by many patients who are intolerant of conventional blockers.

NCT ID: NCT00868855 Terminated - Clinical trials for Coronary Artery Disease

Tissue-Type Plasminogen Activator (t-PA) Release Predicts Major Adverse Cardiac Events (MACE) in Patients With Non-critical Coronary Artery Disease

Start date: December 2003
Phase: Phase 1
Study type: Interventional

Coronary artery disease is the leading cause of death in USA. Contemporary cardiac care has substantially reduced mortality and morbidity in patients with severe coronary artery disease. However, patients with mild to moderate coronary artery stenosis (<70% stenosis) often present in the future with life threatening acute coronary syndrome which carries significant mortality and morbidity. It is difficult to predict outcomes in these patients before the events because the lack of complete understanding of the mechanisms underlying acute coronary syndrome and the lack of reliable markers that will predict major adverse cardiac events (MACE). Tissue-type plasminogen activator (t-PA) is released from endothelial cells and a major factor that prevent thrombosis in the coronary artery, the cause of acute coronary syndrome. Endothelial dysfunction impairs t-PA release. Therefore, we hypothesize that patients with impaired coronary artery t-PA release will have significantly higher risk for future MACE due to intrinsic fibrinolytic dysfunction that leads to increased thrombosis risk. To test this hypothesis, we will determine whether intrinsic endothelial fibrinolytic dysfunction predicts MACE in patients with non-significant CAD. The study will measure t-PA release mediated by bradykinin, a major mediator for t-PA release. This will involve infusion of bradykinin into left main coronary artery of individuals who have undergone routine cardiac catheterization (clinically indicated). We will take blood samples from the coronary sinus and measure t-PA and plasminogen activator inhibitor-1 antigen and activity levels.

NCT ID: NCT00863980 Terminated - Hypertension Clinical Trials

Effects of Telmisartan on Ischemic Cardiovascular Events in High-risk Hypertensive Patients

KCPS
Start date: April 2009
Phase: N/A
Study type: Interventional

This study is aimed to investigate whether treatment with Telmisartan is more effective than Candesartan in reducing the ischemic cardiovascular events in high-risk patients with cardiovascular disease.

NCT ID: NCT00855478 Terminated - Clinical trials for Coronary Artery Disease

French Post-Marketing Surveillance Survey

FR E-REGISTRY
Start date: May 2006
Phase: Phase 4
Study type: Interventional

To assess the safety and effecacy of the Cypher stent ™ & Cypher Select ™ in the normal use of medical practices, within the labeled indications.

NCT ID: NCT00850473 Terminated - Clinical trials for Coronary Artery Disease

PET/CT Study in the Diagnosis of Coronary Plaque

PET/CT
Start date: October 2007
Phase: N/A
Study type: Interventional

This study is being done to determine if a picture taking test of the heart, positron emission tomography/computed tomography (or cardiac PET/CT), can identify the blockages in the heart arteries that lead to heart attacks when compared to the standard of heart catheterization.

NCT ID: NCT00832572 Terminated - Pain Clinical Trials

Study of Ranexa in Patients With Coronary Artery Disease and Painful Polyneuropathy

Start date: January 2009
Phase: Phase 4
Study type: Interventional

This study was to determine whether ranolazine was effective in the treatment of neuropathic pain in patients with coronary artery disease. Eligibility required neurological examination by the study doctor and assessment of the patient's pain. Eligible participants were randomized to receive blinded study medication for a total of 12 weeks.

NCT ID: NCT00808652 Terminated - Clinical trials for Ischemic Heart Disease

Prevalence and Outcome of Brachial Artery Endothelial Function in Morbidly Obese Patients Undergoing Bariatric Surgery

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

The relation between obesity and ischemic heart disease (IHD) is under considerable debate. The reduction in all-cause mortality and, more specifically, the reduction in cardiac-related mortality seen after weight-loss surgery, may be due to regression or slowing developement of subclinical IHD. Function of cells lining the arteries (endothelium) is closely related to the state of IHD and its measurement can serve as a surrogate marker for the existence and severity of IHD. The investigators hypothesize that the prevalence of undiagnosed IHD in the morbidly obese population is high and that following surgery for weight reduction there is a halt in the progression, or even a regression in its severity. The study includes measurement of endothelial function before and after weight-reducing surgery.