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Cardiomyopathies clinical trials

View clinical trials related to Cardiomyopathies.

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NCT ID: NCT00466713 Terminated - Clinical trials for Dilated Cardiomyopathy

Defining the Role of Insulin Resistance in 'Idiopathic' Dilated Cardiomyopathy

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

This study will investigate the effects of rosiglitazone, a medicine commonly used to treat type 2 diabetes, on the utilization of glucose by the heart in patients with heart failure which is not due to heart attacks. The primary purpose of the study is to determine whether treatment with an insulin-sensitizing medication will improve the heart's ability to metabolize glucose (sugar).

NCT ID: NCT00456040 Completed - Cardiomyopathy Clinical Trials

Characteristics of Patients With Amyloidosis & Heart Failure Being Evaluated for a Heart Transplant

Start date: March 2007
Phase: N/A
Study type: Observational

The purpose of this study is to describe the characteristics of patients with amyloidosis and severe heart failure being evaluated for cardiac and stem cell transplantation.

NCT ID: NCT00454818 Completed - Clinical trials for Heart Failure, Congestive

Efficacy and Safety Study of Genetically Targeted Enzyme Replacement Therapy for Advanced Heart Failure

CUPID
Start date: March 2007
Phase: Phase 1/Phase 2
Study type: Interventional

The study is divided into 2 parts. In the first part, the safety of the gene transfer agent MYDICAR® will be evaluated. In the second part, the ability of MYDICAR® to improve heart function will be studied.

NCT ID: NCT00430833 Active, not recruiting - Clinical trials for Hypertrophic Cardiomyopathy

CHANCE - Candesartan in Hypertrophic Cardiomyopathy

Start date: n/a
Phase: Phase 2
Study type: Interventional

The primary hypothesis of the study is that treatment with AT1-R antagonist in patients with nonobstructive form of HCM will be first save, second will cause regression of myocardial hypertrophy.

NCT ID: NCT00428103 Withdrawn - Clinical trials for Congestive Heart Failure

Effects of Mitral Valve Repair With the Geoform Ring on Cardiomyopathy

Start date: October 2006
Phase: N/A
Study type: Interventional

The primary aim of this study is to assess the changes on the shape and function of the left ventricle in patients with severe mitral valve regurgitation due to congestive heart failure and cardiomyopathy who undergo mitral valve reconstruction with a Geoform ring. Three-dimensional echocardiogram will be used for precise evaluation of the shape and function of the ventricle.

NCT ID: NCT00418041 Active, not recruiting - Heart Failure Clinical Trials

Chronic Heart Failure Analysis and Registry in the Tohoku District 2 (CHART-2 Study)

Start date: October 2006
Phase: N/A
Study type: Observational

Chronic Heart Failure Analysis and Registry in the Tohoku District 2 (CHART-2 Study) is a large, prospective, hospital-based cohort study to investigate the following: - Characteristics of patients with chronic heart failure and prognostic risks of these patients. - Characteristics of patients with high risk for heart failure and critical factors which predict the development of symptomatic heart failure in these patients. - The incidence and prognostic impact of metabolic syndrome in patients with chronic heart failure. - The association between metabolic syndrome and the development of symptomatic heart failure.

NCT ID: NCT00401856 Completed - Cardiomyopathy Clinical Trials

CMR to Assess Fibrosis in Cardiomyopathy Using Eplerenone

Start date: December 2007
Phase: Phase 4
Study type: Interventional

The aim of this study is to determine if therapy with the aldosterone antagonist, Eplerenone, is associated with improved remodeling of the left ventricle in patients with cardiomyopathy. We will determine if any benefit to cardiac remodeling is associated with improved clinical outcomes, including improved exercise capacity and reduced incidence of major adverse cardiac events such as death, hospitalization for heart-failure, serious heart rhythm disturbances and transplantation. The null hypothesis is that therapy with Eplerenone over 12 months is associated with an improvement in cardiopulmonary exercise capacity and furthermore that treatment is associated with improved clinical outcomes. In order to test this hypothesis we will study stable patients on optimal drug therapy with documented cardiomyopathy using a trial design where therapy will be randomized, double-blinded and placebo-controlled. This will reduce the likelihood of any 'researcher bias'. Patients will be recruited from the Heart-failure Service at the Royal Brompton Hospital.

NCT ID: NCT00376532 Completed - Arrythmia Clinical Trials

Extracellular Matrix Marker of Arrhythmia Risk (EMMA)

EMMA
Start date: September 2006
Phase: N/A
Study type: Observational

Assess whether serum levels of MMP 2 and or MMP 9 correlate with episodes of ventricular tachycardia or fibrillation in patients who have implantable cardioverter defibrillator devices.

NCT ID: NCT00374465 Recruiting - Clinical trials for Dilated Cardiomyopathy

Therapy With Verapamil or Carvedilol in Chronic Heart Failure

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

The aim of this study is to compare the effect of treatment with verapamil or carvedilol on long-term outcomes in stable, chronic heart failure secondary to non-ischemic cardiomyopathy.

NCT ID: NCT00371891 Completed - Clinical trials for Coronary Arteriosclerosis

Ontario Multidetector Computed Tomographic (MDCT) Coronary Angiography Study (OMCAS)

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

Multidetector Computed Tomographic Coronary Angiography (MDCTCA) has been recently demonstrated to be accurate and may be used as a potential alternative to conventional invasive coronary angiography, which requires cardiac catheterization, for the diagnosis of coronary artery disease. The purpose of this study is to see if MDCTCA can identify significant coronary artery disease as good as or better than conventional coronary angiography (CICA). The study is designed to enroll 900 subjects and is being conducted in 6 hospitals in Ontario. Subjects scheduled for conventional cardiac catheterization and coronary angiography will receive an additional test using MDCTCA. The information gathered during the MDCTCA will be compared to the results of the scheduled conventional invasive coronary angiogram.