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Cardiomyopathy, Dilated clinical trials

View clinical trials related to Cardiomyopathy, Dilated.

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NCT ID: NCT00208806 Completed - Clinical trials for Dilated Cardiomyopathy

Resynchronization Therapy in Young Patients With and Without CHD

Start date: June 2004
Phase: N/A
Study type: Observational

Pacemakers can be attached to one or more than one of the heart chambers. After watching pacemakers work over time, doctors have found that the pacemakers that stimulate only one chamber of the heart sometimes lead to problems later. These problems may be changes in the size and shape of the heart. The heart cannot work as well when some of these changes happen. We need to learn more about these changes and how to prevent them. There has not been an easy way to do this. A new treatment called Cardiac Resynchronization Therapy (CRT) is associated with biventricular pacing where two chambers of the heart are stimulated simultaneously. Tissue Doppler Imaging,Tissue Synchronization Imaging and 3 dimensional echocardiography are new forms of technology that look at the heart while it works. They are similar to a moving x-ray that can watch the heart muscles moving. The movement can be measured. Doctors will check for changes that happen over time. This has not been studied in children before because this kind of is new to this group of patients. This technology is noninvasive which means it can be done from the outside of the body and is painless. The hearts of children grow fast. It is important to be able to know if the pacemaker or problems from dilated cardiomyopathy are causing any changes in the heart that might cause problems. We expect to be able to use information we learn from this study to improve how we use pacemakers in the future to avoid problems that can happen over time.

NCT ID: NCT00180323 Completed - Clinical trials for Dilated Cardiomyopathy

ACC - Atrial Contribution to CRT

Start date: November 2004
Phase: N/A
Study type: Interventional

This prospective study will evaluate in patients, fulfilling implant criteria for Cardiac Resynchronisation Therapy (CRT) implant, the optimal atrial contribution to the resynchronised ventricles in the event of right atrial pacing.

NCT ID: NCT00123071 Completed - Clinical trials for Cardiomyopathy, Dilated

Variability of Ventricular Mass, Volume, & Ejection Fraction in Pediatric Cardiomyopathy Patients-Pediatric Heart Network

VVV
Start date: May 2005
Phase: N/A
Study type: Observational

This observational study will provide data (variations in ventricular size and function) that are essential to designing and conducting clinical trials. In addition, the study will evaluate intra- and inter-study variability seen in echocardiography.

NCT ID: NCT00046618 Completed - Clinical trials for Cardiovascular Diseases

Mapping Novel Disease Genes for Dilated Cardiomyopathy

Start date: July 2002
Phase: N/A
Study type: Observational

To identify new dilated cardiomyopathy genes by genetic linkage and mutational analyses.

NCT ID: NCT00005262 Completed - Hypertension Clinical Trials

Epidemiology of Idiopathic Dilated Cardiomyopathy (Washington, DC Dilated Cardiomyopathy Study)

Start date: July 1990
Phase: N/A
Study type: Observational

To identify risk factors for idiopathic dilated cardiomyopathy and to examine prognostic factors over a follow-up period of two to three years.

NCT ID: NCT00005201 Completed - Heart Diseases Clinical Trials

Idiopathic Dilated Cardiomyopathy

Start date: July 1987
Phase: N/A
Study type: Observational

To determine the familial occurrence and pathogenesis of idiopathic dilated cardiomyopathy.

NCT ID: NCT00005156 Completed - Hypertension Clinical Trials

Mortality Surveillance of MRFIT Screenees

Start date: April 1982
Phase: N/A
Study type: Observational

To ascertain the sixteen year mortality status of the 361,662 middle-aged men screened in 1973-1975 for the Multiple Risk Factor Intervention Trial (MRFIT).

NCT ID: NCT00001402 Completed - Clinical trials for Heart Failure, Congestive

PET Scan to Determine Areas of Blood Flow and Activity in the Hearts of Patients With Heart Disease Taking Beta-Blockers

Start date: January 1994
Phase: Phase 2
Study type: Interventional

The human heart is divided into four chambers. One of the four chambers, the left ventricle, is the chamber mainly responsible for pumping blood out of the heart into the circulation. Diseases of the heart like congestive heart failure (CHF), can cause the left ventricle to function improperly. Medications called beta-blockers appear to reverse the abnormalities in the left ventricle and frequently improve the function of the left ventricle in patients with different kinds of heart disease. How beta-blockers improve left ventricle function is unknown. One possible reason for improved function of the left ventricle with beta-blockers is improved blood flow to the heart muscle. When a region of the heart is active, it uses more fuel in the form of oxygen and sugar (glucose). As heart activity increases, blood flow to and from the area of activity increases also. Knowing these facts, researchers can use radioactive sugar (glucose) and positron emission tomography (PET) scans to observe what areas of the heart are receiving more blood flow. In this study researchers plan to measure glucose use in heart muscle and blood flow to the heart muscle in patients with CHF taking beta-blockers.

NCT ID: NCT00001313 Completed - Heart Failure Clinical Trials

Evaluation of Patients With Known or Suspected Heart Disease

Start date: May 10, 1992
Phase: N/A
Study type: Observational

In this study researchers will admit and evaluate patients with known or suspected heart disease referred to the Cardiology Branch of the National Heart, Lung, and Blood Institute (NHLBI). Patients participating in this study will undergo a general medical evaluation, including blood tests, urine, examination, chest x-ray and electrocardiogram (EKG). In addition, patients may be asked to have an echocardiogram (ultrasound scan of the heart) and to perform an exercise stress test. These tests are designed to assess the types and causes of patient's heart diseases and to determine if they can participate in other, specific research studies.