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Ischemia clinical trials

View clinical trials related to Ischemia.

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NCT ID: NCT00588042 Completed - Clinical trials for Coronary Artery Ischemia

Remote Myocardial Ischemic Preconditioning in Humans

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

Ischemic preconditioning (IP) has been shown in animal studies to increase the myocardial tolerance to subsequent ischemia. Our primary hypothesis is that remote IP reduces myocardial ischemic injury during PCI.

NCT ID: NCT00585663 Completed - Clinical trials for Coronary Artery Disease

Accuracy of Radiolabeled Fatty Acid Analog, BMIPP, in the Late Detection of Decreased Blood Flow to the Heart

ZEUSS-ACS
Start date: August 2007
Phase: Phase 2
Study type: Interventional

The purpose of this study is to: - evaluate the performance characteristics (sensitivity & specificity) of iodofiltic acid I-123 imaging for detection of myocardial ischemia in patients that present in the Emergency Department with suspected Acute Coronary Syndrome (ACS). - evaluate the safety of a single injection of iodofiltic acid I-123 in patients suspected of myocardial ischemia related to ACS.

NCT ID: NCT00574847 Completed - Myocardial Ischemia Clinical Trials

Responses of Myocardial Ischemia to Escitalopram Treatment

REMIT
Start date: September 2006
Phase: Phase 4
Study type: Interventional

Depression is commonly seen in patients with cardiovascular disorders. In recent studies it has been shown that mild to moderate depression symptoms were associated with increased likelihood of mental stress-induced myocardial ischemia (MSIMI), which is a risk factor of poor cardiac outcome. In this project, the investigators aim to assess the treatment of mental stress-induced myocardial ischemia in ischemic heart disease patients with mild to moderate depressive symptoms. This study is a six-week double-blind placebo controlled study to examine the effects of escitalopram on mental stress-induced myocardial ischemia. This study will look to show that patients with ischemic heart disease who are treated with escitalopram will exhibit a significant improvement of MSIMI at the end of week 6 compared to patients receiving placebo.

NCT ID: NCT00570089 Completed - Myocardial Ischemia Clinical Trials

Microvascular Coronary Disease In Women: Impact Of Ranolazine

Start date: April 2007
Phase: Phase 2
Study type: Interventional

1. To evaluate the impact of ranolazine extended-release tablets in women with subendocardial ischemia due to microvascular endothelial dysfunction on myocardial ischemia (Cardiac Magnetic Resonance (CMR) extent, severity. 2. To evaluate the impact of ranolazine extended-release tablets in women with subendocardial ischemia due to microvascular endothelial dysfunction on the outcomes of angina (Seattle Angina Questionnaire (SAQ), WISE angina frequency, Duke Activity Status Inventory(DASI) and SF-36).

NCT ID: NCT00569621 Completed - Ischemia Clinical Trials

A Randomized, Double-Masked, Placebo-Controlled Two Cross Over Study Comparing the Effects of Moxaverine and Placebo on Ocular Blood Flow

Start date: March 2007
Phase: Phase 2
Study type: Interventional

It is known that several common eye diseases are associated with ocular perfusion abnormalities. Moxaverine is used in the therapy of perfusion abnormalities in the brain, the heart and the extremities because of its direct vasodilatory effects. The present study seeked to investigate whether moxaverine alters ocular blood flow in healthy volunteers after intravenous administration.

NCT ID: NCT00568542 Completed - Clinical trials for Ischemic Cardiomyopathy

Chronic, Low Dose Erythropoetin Beta in Ischemic Cardiomyopathy

EPOHeart
Start date: May 2006
Phase: Phase 4
Study type: Interventional

The study is testing the hypothesis, that the application of low dose erythropoetin beta (35 I.E./kg BW/week) for 6 months following successful coronary revascularization by PCI improves left ventricular remodeling as assessed by cardiac MRI.

NCT ID: NCT00564382 Completed - Clinical trials for Magnetic Resonance Imaging

CMR in the Assessment of Patient With ACS in the Emergency Room

Start date: November 2007
Phase: N/A
Study type: Interventional

In this study, we investigate the role of Cardiac Magnetic Resonance Imaging in patients with suspected, but not yet proven, "acute cardiac syndrome ACS". Patients are included if they presented to the local Emergency Department with chest pain, but the first tests in the Emergency Department are negative or not clearly indicative of cardiac ischemia. For example, the first lab value Troponin T is negative or borderline elevated; or the first ECG is not clearly indicative of ischemia. The standard procedure for these patients is to wait 4-6 hours and then repeat the test; if they continue to be negative, the patients are discharged home, if the have become positive, an invasive coronary artery angiography has to be performed. We think, that a CMR study can shorten the time needed to make the decision of either "discharge" or "admit to CCU and perform a coronary artery angiography". CMR has been shown to be the gold standard for heart function (thus, can see even subtle wall motion abnormalities), for tissue characterization (so-called T2-weighted images can identify tissue edema (swelling); perfusion images can identify areas with reduced blood supply; late enhancement images can safely identify fibrotic or irreversibly damaged tissue) and can even be used to stress the patients to exclude a critical or non-critical narrowing of coronary arteries. The primary endpoint of this study will be the impact of CMR on the time-to-decision in these patients. It should be possible to a) identify all patients WITH an acute infarct by CMR and send them to a cath lab sooner compared to waiting for a second test; b) identify all patients WITHOUT an acute infarct and c) perform a stress test in those patients to exclude severe coronary artery disease.

NCT ID: NCT00563238 Withdrawn - Myocardial Ischemia Clinical Trials

Beta-blocker Before Extubation

Start date: November 2007
Phase: N/A
Study type: Interventional

Silent myocardial ischemia is known to occur in the general medical intensive care unit population immediately following tracheal extubation. We believe these patients are at risk for primary cardiac events in the 4 hours immediately following extubation. Metoprolol is a selective beta-1 antagonist, with little to no beta-2 activity at low and moderate doses. The cardioprotective effects of beta blockade have been well documented in randomized controlled trials. In patients undergoing extubation, prophylactic use of intravenous metoprolol may reduce post-extubation ischemia events as well as precursors of cardiogenic pulmonary edema (atrial and ventricular wall tension). Our primary hypothesis is that prophylactic metoprolol (titrated to reduce resting heart rate by at least 10%) prior to tracheal extubation will reduce the rate of ischemia as judged by ST segment analysis.

NCT ID: NCT00561834 Completed - Clinical trials for Nonarteritic Anterior Ischemic Optic Neuropathy

Ranibizumab Therapy for Non-arteritic Ischemic Optic Neuropathy

NAION
Start date: November 2007
Phase: Phase 1
Study type: Interventional

The purpose of this study is to explore the safety and efficacy of ranibizumab to treat non-arteritic ischemic optic neuropathy based on clinical and anatomical findings.

NCT ID: NCT00558857 Terminated - Clinical trials for Ischemic Ventricular Tachycardia

Dynamic Substrate Mapping (DSM) for Ischemic VT

DSM
Start date: July 2007
Phase: Phase 1
Study type: Interventional

This is a prospective, non-randomized study to determine the feasibility of using a new technique called Dynamic Substrate Mapping (DSM) to help guide the treatment of ischemic ventricular tachycardia (IVT). We hypothesize that DSM will lead to simpler, more effective ablation of IVT. Results from this study will be used to determine if further clinical investigation is warranted.