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Cardiomyopathies clinical trials

View clinical trials related to Cardiomyopathies.

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NCT ID: NCT00629018 Completed - Clinical trials for Dilated Cardiomyopathy

Safety and Efficacy Study of Stem Cell Transplantation to Treat Dilated Cardiomyopathy

Start date: May 2006
Phase: Phase 2
Study type: Interventional

Several studies have documented that transplantation of bone marrow-derived cells (BMC) following acute myocardial infarction is associated with a reduction in infarct scar size and improvements in left ventricular function and perfusion. The available evidence in humans suggests that BMC transplantation is associated with improvements in physiologic and anatomic parameters in both acute myocardial infarction and chronic ischemic heart disease, above and beyond the conventional therapy. In particular, intracoronary application of BMC is proved to be safe and was associated with significant improvement in the left ventricular ejection fraction (LVEF) in patients with chronic heart failure. In contrast to ischemic heart failure, the data on effects of BMC transplantation in patients with dilated cardiomyopathy are limited to pre-clinical studies. In a rat model of dilated cardiomyopathy, intramyocardial delivery of pluripotent mesenchymal cells improved LVEF, possibly through induction of myogenesis and angiogenesis, as well as by inhibition of myocardial fibrosis, suggesting that the beneficial effects of stem cell transplantation in dilated cardiomyopathy may primarily be related to their ability to supply large amounts of angiogenic, antiapoptotic, and mitogenic factors. Similarly, transplantation of cocultured mesenchymal stem cells and skeletal myoblasts was shown to improve LVEF in a murine model of Chagas disease. Study Aim: To define the clinical effects of BMC transplantation in dilated cardiomyopathy in a pilot clinical study investigating the effects of intracoronary CD34+ cell transplantation on functional, structural, neurohormonal, and electrophysiologic parameters in patients with end-stage dilated cardiomyopathy.

NCT ID: NCT00628056 Recruiting - Clinical trials for Diabetic Cardiomyopathy

Mechanisms Responsible for Cardiac and Skeletal Muscle Energetic Impairment in Diabetes

DDCM
Start date: October 2006
Phase: Phase 1/Phase 2
Study type: Interventional

Diabetes increases the risk of heart failure. This is mainly due to a disease of the blood vessels supplying the heart muscle and/or high blood pressure, but abnormal metabolism may also contribute. We plan to study the mechanisms involved in this abnormal metabolism, whilst also assessing the effects of a drug called Perhexiline which improves the abnormal metabolism that is present in diabetic patients before the development of heart failure.

NCT ID: NCT00626314 Not yet recruiting - Clinical trials for Ischemic Cardiomyopathy

Study to Assess the Efficacy and Safety of Transplanting Autologous Skeletal Myoblasts, Into Infarcted Heart, Using an Catheter Delivery System

CAuSMIc II
Start date: March 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety and effectiveness of injecting myoblasts (grown from your own skeletal muscle), using a catheter device, directly into the damaged heart muscle for treatment of severe heart failure.

NCT ID: NCT00626028 Completed - Cardiomyopathy Clinical Trials

Comparison of Inhaled Nitric Oxide and Oxygen in Participants Reactivity During Acute Pulmonary Vasodilator Testing

Start date: September 2004
Phase: Phase 3
Study type: Interventional

The primary purpose of this study is to compare the number of participants with reversible pulmonary hypertension (vasoreactivity) due to nitric oxide for inhalation and oxygen as compared to 100% oxygen.

NCT ID: NCT00624520 Terminated - Stress Clinical Trials

Mental Stress Reduction in Defibrillator Patients

Start date: September 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the effectiveness of a 10 week program of Stress Management versus control Patient Education sessions on cardiac responses to mental stress in veterans with Implantable Cardioverter-Defibrillators

NCT ID: NCT00622102 Completed - Atrial Fibrillation Clinical Trials

Testing Strategies to Improving Warfarin Adherence

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

We are performing a research study to learn more about the control of an individual's blood thinning (anticoagulation) on warfarin. Individuals from an anticoagulation clinic are being asked to participate in order to see if a lottery which provides the opportunity to win money in combination with the use of the Med-eMonitor might be useful in helping patients to achieve better control of their anticoagulation therapy. Half of the participants will be enrolled in the lottery arm and the other half will be a control group who will receive the Med-eMonitor only.

NCT ID: NCT00615394 Completed - Clinical trials for Dilated Cardiomyopathy

Autologous Transplantation of Bone Marrow Mononuclear Stem-Cells by Mini-Thoracotomy

STEMDILCARD
Start date: April 2004
Phase: Phase 1/Phase 2
Study type: Interventional

Bone marrow mononuclear cells (BMMC) transplantation is a promising therapy for treating ischemic disease, however the effect in non-ischemic dilated cardiomyopathy is unknown.This study describes a technique of BMMC transplantation utilizing mini-thoracotomy and results up to one year after the procedure.

NCT ID: NCT00612911 Terminated - Clinical trials for Cardiomyopathy, Dilated

Cell Therapy in Dilated Cardiomyopathy: Observational Study

Start date: February 2005
Phase: N/A
Study type: Observational

Using bone marrow mononuclear cell in 24 patients with Idiopathic dilated cardiomyopathy

NCT ID: NCT00610896 Completed - Cardiomyopathy Clinical Trials

CRM and Fusion Beats: Effects of Progressive Fusion on Intra-left Ventricular Mechanical Function

Start date: January 2008
Phase: N/A
Study type: Observational

This study is looking at cardiac rhythm management (CRM) and fusion beats in patients who have a pacemaker or implantable cardioverter-defibrillator (ICD), to determine if there is a correlation between the time between the contraction of the upper chambers of the heart (atrium) and the lower chambers of the heart, (ventricle) and heart function. Some studies of people with pacemakers have been done to determine if shortening the time of contraction between the atrium and ventricle could benefit the function of the left ventricle. These studies have shown that there is no benefit in heart function.There have been other studies which have shown that chronic pacing of the right ventricle, especially with the lead placed at the tip of the right ventricle, can lead to a decrease in the function of the left ventricle and congestive heart failure. In some patients long term pacing of the right ventricle has also been associated with a reduction in the ability of the left ventricle to pump blood. This is know as a reduced left ventricular ejection fraction, which can be documented by an echocardiogram. This study proposes to evaluate the acute effects of progressive paced fusion beats on the left ventricle to answer the question whether there is an delay between the atrium and ventricle that is "too long" or "too short".

NCT ID: NCT00606775 Recruiting - Clinical trials for Duchenne Muscular Dystrophy

The Preventive Efficacy of Carvedilol on Cardiac Dysfunction in Duchenne Muscular Dystrophy

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

Purpose This cardiac dysfunction in patients with Duchenne muscular dystrophy is associated with minor cardiac damage as indicated by elevation of plasma cardiac troponin I (cTnI). The purpose of this study is to investigate whether the administration of Carvedilol can suppress the minor cardiac damage and prevent deterioration of cardiac function.