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Ischemic Cardiomyopathy clinical trials

View clinical trials related to Ischemic Cardiomyopathy.

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NCT ID: NCT01557465 Completed - Heart Failure Clinical Trials

Mechanical Alternans Study

MAS
Start date: November 2009
Phase: N/A
Study type: Observational

The purpose of this study is to determine whether mechanical alternans (alternating strong and weak heart beats with a constant beat-to-beat interval), can be used to predict malignant ventricular arrhythmias, requiring defibrillation or appropriate ICD therapies, and to predict progression of heart failure and death.

NCT ID: NCT01496209 Withdrawn - Clinical trials for Ischemic Cardiomyopathy

REgenerative CardiOsphere iNjection to STRengthen dysfUnCTional Hearts

RECONSTRUCT
Start date: July 2015
Phase: Phase 1
Study type: Interventional

A double blinded and placebo-controlled, dose escalation, single-center safety and preliminary efficacy study of cardiospheres delivered via NOGA MYOSTAR injection catheter in subjects with chronic ischemic cardiomyopathy. The objective is to achieve and document myocardial regeneration in patients with chronic scar.

NCT ID: NCT01474486 Completed - Clinical trials for Congestive Heart Failure

Feasibility and Effectiveness of Micronutrients as Palliative Care Therapy in Patients With Congestive Heart Failure

Start date: April 2010
Phase: N/A
Study type: Interventional

The purpose of this project is to conduct a preliminary test of the feasibility of a multi-micronutrient intervention to improve micronutrient status, cardiac function and quality of life in Veterans with Congestive Heart Failure (CHF).

NCT ID: NCT01447069 Not yet recruiting - Heart Failure Clinical Trials

Use of Beta-agonists in Stable Severe Congestive Heart Failure

Start date: October 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether Salbutamol is effective in the treatment of severe heart failure due to ischemic and non- ischemic cardiomyopathy.

NCT ID: NCT01400334 Completed - Clinical trials for Ischemic Cardiomyopathy

Prediction of ARrhythmic Events With Positron Emission Tomography

PAREPET
Start date: July 2004
Phase:
Study type: Observational

The hypothesis of PAREPET is that hibernating myocardium (viable myocardium with reduced resting flow) and/or viable but denervated myocardium can predict the risk of sudden death in subjects with ischemic cardiomyopathy.

NCT ID: NCT01290822 Terminated - Clinical trials for Dilated Cardiomyopathy

Optimized Biventricular Pacing Allograft Recipients

BiBET
Start date: January 2007
Phase: Phase 1/Phase 2
Study type: Interventional

This study tests optimization of biventricular pacing (BiVP) in patients with dilated cardiomyopathy (DCM) or ischemic cardiomyopathy (ICM) during cardiac transplantation in patients with advanced cardiac failure. It examines the effects of atrioventricular delay (AVD), interventricular delay (VVD or RLD), and left ventricular pacing site (LVPS) on cardiac output (CO). BiVP results are compared to traditional atrial (AAI) pacing at an identical heart rate.

NCT ID: NCT01288560 Completed - Clinical trials for Coronary Artery Disease

IMAGE-HF Project I-A: Cardiac Imaging in Ischemic Heart Failure (AIMI-HF)

AIMI-HF
Start date: January 2011
Phase: N/A
Study type: Interventional

Medical imaging is one of the fastest growing sectors in health care and increases in utilization underscore the need to ensure imaging technology is developed and used effectively. Evaluation of the clinical and economic impact of such imaging lags behind the technology development. Heart failure (HF) represents the final common pathway for most forms of heart disease and morbidity and mortality remain high. There is a need to identify imaging approaches that have a positive impact on therapy decisions, patient outcomes and costs. As well as standard methods to evaluate new and emerging techniques to better test their potential in a clinical management setting. PRIMARY OBJECTIVES: to compare the effect of HF imaging strategies on the composite clinical endpoint of cardiac death, MI, resuscitated cardiac arrest and cardiac re-hospitalization (WHF, ACS, arrhythmia). Patients with an ischemic heart disease (IHD) etiology will follow HF imaging strategy algorithms according to the question(s) asked by the physicians (is there ischemia and/or viability), in agreement with their local practices for standard and alternative imaging. SECONDARY OBJECTIVES: 1. To evaluate the effect of imaging modalities within and between the imaging subgroups (advanced (CMR and PET), PET, MRI and standard (SPECT)) on the primary and secondary outcomes in patients being evaluated either for viability and/or ischemia. 2. To evaluate the impact of adherence to recommendations between modalities on outcomes in patients being evaluated for either viability or ischemia. 3. To compare the effect of HF imaging strategies on: 1. The incidence of revascularization procedures (PCI, CABG, none) and the interaction of the imaging strategy and types of revascularization on outcomes 2. LV remodeling: LV volumes, LVEF, 3. HF symptoms, NYHA class 4. QOL (MLHFQ, the EQ5D) 5. The evolution of serum prognostic markers in HF (e.g. BNP, RDW, hs-cTnT, hs-CRP, ST2) 6. Health economics: Costs estimated through regression analysis and cost effectiveness assessed through decision modeling. 7. The safety of imaging tests measured by cumulative radiation, adverse reactions to imaging contrast agents and stress testing agents will also be determined. 8. The evolution of renal function (eGFR) and LV remodeling-associated biomarkers (e.g. PIIINP, OPN). 9. Event rates of each component of the composite endpoint as well as the combined endpoint of CV death and HF hospitalization 10. All-cause mortality

NCT ID: NCT01215253 Completed - Heart Failure Clinical Trials

Ranolazine Implantable Cardioverter-Defibrillator Trial

RAID
Start date: September 2011
Phase: Phase 3
Study type: Interventional

The purpose of the study is to see how effective a drug called ranolazine is in reducing the risk of ventricular arrhythmia and death in people with implantable cardioverter-defibrillators (ICDs). This drug will be used with standard medications that is routinely prescribed in enrolled patients.

NCT ID: NCT01076660 Recruiting - Clinical trials for Ischemic Cardiomyopathy

Left Ventricular Structural Predictors of Sudden Cardiac Death

Start date: October 2003
Phase:
Study type: Observational

Sudden cardiac death (SCD) poses a significant health care challenge with high annual incidence and low survival rates. Implantable cardioverter defibrillators (ICDs) prevent SCD in patients with poor heart function. However, the critical survival benefit afforded by the devices is accompanied by short and long-term complications and a high economic burden. Moreover, in using current practice guidelines of reduced heart function, specifically left ventricular ejection fraction (LVEF)≤35%, as the main determining factor for patient selection, only a minority of patients actually benefit from ICD therapy (<25% in 5 years). There is an essential need for more robust diagnostic approaches to SCD risk stratification. This project examines the hypothesis that structural abnormalities of the heart itself, above and beyond global LV dysfunction, are important predictors of SCD risk since they indicate the presence of the abnormal tissue substrate required for the abnormal electrical circuits and heart rhythms that actually lead to SCD. Information about the heart's structure will be obtained from cardiac magnetic resonance imaging and used in combination with a number of other clinical risk factors to see if certain characteristics can better predict patients at risk for SCD.

NCT ID: NCT01019226 Recruiting - Clinical trials for Ischemic Cardiomyopathy

Implementation of Work in Progress (WIP) Sequences in Magnetic Resonance Imaging (MRI)

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

Trial of new work in progress (WIP) sequences in MRI.