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Cardiomyopathies clinical trials

View clinical trials related to Cardiomyopathies.

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NCT ID: NCT00505154 Completed - Clinical trials for Dilated Cardiomyopathy

Effect of Rosuvastatin on Left Ventricular Remodeling

Start date: July 2007
Phase: Phase 3
Study type: Interventional

The purpose of this study is to examine the the effect of the HMG-CoA reductase inhibitor Rosuvastatin on left ventricular remodeling in patients with dilated cardiomyopathy.

NCT ID: NCT00504647 Recruiting - Clinical trials for Hypertrophic Cardiomyopathy

Biventricular Pacing in Hypertrophic Cardiomyopathy

Start date: June 2006
Phase: Phase 1
Study type: Interventional

Hypertrophic Cardiomyopathy is an inherited condition characterized by thickening (hypertrophy) of the heart muscle. Many patients who have this condition have a reduced ability to exercise because of breatlessness, which can in some cases be severe. This appears in most cases to be due to an impairment of the filling of the heart, especially on exercise this limits the amount of blood the heart is able to pump. Several factors may contribute to this slow filling of the heart, including (1) The heart contracts and relaxes in an incoordinate way (called 'dyssynchrony') which is inefficient, and (2) The filling of the main pumping chamber (the left ventricle) may be impeded by high pressure in the other ventricle(the right ventricle)- in other words the left ventricle is 'squashed' by the right ventricle. This is known as diastolic ventricular interaction. Although drugs can improve the filling of the heart and relieve symptoms, some patients remain very symptomatic despite these drugs. The mechanisms responsible for the filling abnormality in patients with Hypertrophic Cardiomyopathy are similar to those seen in the much more common condition known as Heart Failure. A special type of pacemaker technique called 'Biventricular Pacing' has been shown to markedly improve symtoms in patients with heart failure. This form of pacing has been shown to improve both 'dyssynchrony' ( incoordination) and 'ventricular interaction' (squashed left heart) in patients with Heart Failure. We propose that Biventricular pacing may similarly improve these abnormalities in patients with Hypertrophic Cardiomyopathy, resulting in an improvement of symptoms. The study will focus on patients with the condition who have severe symtoms despite being on optimal currently available drug therapy.

NCT ID: NCT00500734 Recruiting - Heart Disease Clinical Trials

Cardiomyopathy Tissue Bank in a Cancer Population

Start date: December 10, 2002
Phase:
Study type: Observational

Any time the words "you," "your," "I," or "me" appear, it is meant to apply to the potential participant. The goal of this laboratory research study is to collect and store blood and tissue from patients who have a diagnosis of heart disease and may be at a high risk for the development of heart failure. This blood may be used in the future to identify genes that may play a role in developing congestive heart failure (CHF) from chemotherapy or other sources. This is an investigational study. All will be enrolled at MD Anderson.

NCT ID: NCT00500552 Completed - Clinical trials for Hypertrophic Cardiomyopathy

Perhexiline Therapy in Patients With Hypertrophic Cardiomyopathy

METAL-HCM
Start date: December 2006
Phase: Phase 2
Study type: Interventional

Hypertrophic Cardiomyopathy (HCM) is a relatively common inherited heart muscle disease. Many patients experience symptoms of breathlessness, fatigue and chest pain. These symptoms are not always controlled with current therapies. Recently the investigators showed that a drug called Perhexiline markedly improved exercise capacity and symptoms in patients with heart failure. In this proposal the investigators wish to test whether Perhexiline improves exercise capacity and relieves symptoms in patients with HCM

NCT ID: NCT00490347 Completed - Cardiomyopathies Clinical Trials

VentrAssistTM LVAD as a Bridge to Cardiac Transplantation - Feasibility Trial

Start date: July 2005
Phase: Phase 2
Study type: Interventional

The purpose of this trial is to determine the safety and feasibility of the VentrAssist LVAD in providing circulatory support for patients who require an LVAD as a bridge to cardiac transplantation.

NCT ID: NCT00490321 Active, not recruiting - Cardiomyopathies Clinical Trials

VentrAssistTM LVAD for the Treatment of Advanced Heart Failure - Destination Therapy

Start date: June 2007
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the safety and effectiveness of LVADs in providing long-term circulatory support for patients who have chronic stage D heart failure and are ineligible for a heart transplant. This is a multi-center, prospective, randomized, controlled clinical trial, which is comprised of two independent modules.

NCT ID: NCT00489957 Completed - Cardiomyopathy Clinical Trials

Speckle Tracking in Pediatric Patients

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

An echocardiogram, also called a cardiac ultrasound or echo, is a medical test that takes pictures of the heart using sound waves. It shows images of the structures of the heart without using radiation. During the last year, the FDA has approved a new technology called Speckle Tracking that can look at the heart wall motion and contraction (pumping or squeezing) abnormalities. The study will also employ tissue Doppler and 3-Dimensional echo and uses the same echocardiographic machines which are used right now. The machines are upgraded with the new software application. This new technology is currently being used in adults, but unfortunately, there is almost no published data about normal heart function in infants and children using this technology. It is known from other technologies that the developing child's heart is not the same as an adult. The investigators wish to study this new technology and compare it to other technologies currently being used.

NCT ID: NCT00483236 Withdrawn - Clinical trials for Congestive Heart Failure

Prospective Study Looking at Quality of Life Measures in Non-ischaemic Cardiomyopathy After Mitral Valve Repair

Start date: December 1, 2007
Phase:
Study type: Observational

- Chronic severe mitral regurgitation can lead to symptoms and left ventricular dysfunction. - The purpose of this study is to prospectively follow patients with non-ischaemic cardiomyopathy who are eligible for mitral valve repair surgery and primarily measure the quality of life through the Minnesota Living with Heart Failure Questionnaire & the Kansas City Cardiomyopathy Questionnaire.

NCT ID: NCT00483197 Active, not recruiting - Cardiomyopathies Clinical Trials

VentrAssistTM LVAD as a Bridge to Cardiac Transplantation - Pivotal Trial

Start date: June 2007
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the safety and effectiveness of VentrAssistTM LVAD in individuals who are awaiting heart transplants.

NCT ID: NCT00474461 Completed - Clinical trials for Coronary Artery Disease

Cardiac Stem Cell Infusion in Patients With Ischemic CardiOmyopathy (SCIPIO)

SCIPIO
Start date: February 2009
Phase: Phase 1
Study type: Interventional

The purpose of this study is to investigate the safety of intracoronary cardiac stem cells (CSCs) therapy in humans. Currently, there is no effective intervention to regenerate (regrow) dead heart muscle after a heart attack. The central hypothesis is that CSCs infused into nonviable myocardial segments will regenerate infarcted myocardium by differentiating into cardiomyocytes and other cell types. According to our hypothesis, CSC infusion regenerates myocardium with consequent improvement in contractile function of the heart and general clinical status.