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Ventricular Dysfunction, Left clinical trials

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NCT ID: NCT01178866 Completed - Clinical trials for Left Ventricular Dysfunction

Laboratory Outcome Predictors in Coronary Surgery

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

Evaluate less employed markers of tissue hypoperfusion as venoarterial carbon dioxide partial pressure difference (ΔPCO2) and estimated respiratory quotient (eRQ) combined to other classically studied markers as predictive factors of complicated clinical course after cardiac surgery in patients with left ventricular dysfunction.

NCT ID: NCT01162083 Completed - Clinical trials for Mitral Regurgitation

Identifying an Ideal Cardiopulmonary Exercise Test Parameter

PVA
Start date: October 2010
Phase: N/A
Study type: Observational

Cardiopulmonary exercise testing (CPET) is a safe, noninvasive investigation where a patient walks on a treadmill or cycles whilst attached to an ECG and with a mask that measures the air breathed in and out. It has numerous clinical uses, such as diagnosing the main cause in patients with breathlessness, deciding on timing for heart transplantation and assessing whether patients are safe for a general anaesthetic. A patient's peak oxygen consumption, the maximum amount of oxygen taken up by the blood from the lungs when breathing increases during exercise, is the main measurement taken from CPET. It is low in heart disease and has been used to predict the risk of death and therefore plan treatments for patients. However this is also low in numerous other diseases including lung disease; reduced oxygen consumption in patients with two conditions may be wrongly thought to be because of the heart leading to inappropriate action and distress to the patient. Newer measurements of exercise capacity from the same exercise test are better at predicting death in heart failure. We propose that they are more specific for heart failure over other diseases, for example lung disease, when compared with peak oxygen consumption, and are superior when a single best test for heart failure is required. This research aims to identify which measurement of exercise capacity is most specific for heart failure. We will perform the test on many patients with different diseases, and before and after procedures such as the implantation of special pacemakers, and heart valve operations. This should lead to a more accepted use of this investigation and the more appropriate identification of which patient should have which procedure.

NCT ID: NCT01128790 Completed - Heart Failure Clinical Trials

Pilot Study of Remote Ischemic Preconditioning in Heart Failure

Start date: October 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the effect of remote ischemic preconditioning on exercise capacity in patients with heart failure.

NCT ID: NCT01110824 Completed - Multiple Myeloma Clinical Trials

Prevention of Left Ventricular Dysfunction During Chemotherapy

OVERCOME
Start date: April 2008
Phase: Phase 3
Study type: Interventional

The investigators' objective is to assess the efficacy of the combined treatment with enalapril and carvedilol in the prevention of left ventricular systolic dysfunction in patients with hematological malignancies submitted to intensive chemotherapy with potential cardiotoxicity. The hypothesis is that these drugs administered during chemotherapy may prevent left ventricular systolic dysfunction.

NCT ID: NCT01110395 Completed - Clinical trials for Left Ventricular Dysfunction

Phosphorous Magnetic Resonance Spectroscopy of Heart

Start date: June 2009
Phase: N/A
Study type: Interventional

Heart needs constant supply of energy to continue working. Phosphorus magnetic resonance spectroscopy allows us to measure energy produced in the heart. The purpose of this study is to determine if the energy production is reduced in failing heart.

NCT ID: NCT01093001 Completed - Clinical trials for Left Ventricular Dysfunction

Tricuspid Regurgitation Study

Start date: May 2010
Phase: Phase 4
Study type: Interventional

The effect of cardiac pacing leads on tricuspid regurgitation is unclear. This study will determine whether using a smaller diameter leads and an alternate position in the ventricle, the proximal septum, will reduce tricuspid regurgitation than larger leads placed in the apex.

NCT ID: NCT01086124 Completed - Clinical trials for Myocardial Infarction

Objective Systolic Function Recuperation Assessed by Echocardiography

ROSE
Start date: March 2010
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate left ventricular systolic ejection fraction and anterior or apical akinesis 1 month and 3 months after a myocardial infarction treated with primary PCI to determine whether improvement at 1 month differs from improvement at 3 months.

NCT ID: NCT01076920 Completed - Clinical trials for Left Ventricular Dysfunction

Mesenchymal Stem Cells and Myocardial Ischemia

MESAMI
Start date: October 2009
Phase: Phase 1/Phase 2
Study type: Interventional

Ischemic cardiomyopathies are a leading cause of death in both men and women. When a person has a heart attack, blood is unable to reach a certain area of the heart, and if the blood supply is not re-established quickly, that area of the heart can suffer permanent damage. While recovery from a heart attack can be managed through medications and lifestyle changes, these treatments can not reverse the all damage to the heart. Current research is focusing on the development of cell-based therapies using stem cells to repair organs that have been irreversibly damaged by disease. A specific form of stem cells, called adult mesenchymal stem cells (MSCs), has shown promise for heart repair. This study will evaluate the safety of injecting MSCs directly into the heart to repair and restore heart function in people who have had a heart attack and who have chronic myocardial ischemia with heart failure.

NCT ID: NCT01076296 Completed - Clinical trials for Pulmonary Hypertension

A Post-Marketing Study for On Label Evaluation of the GE Vscan Ultrasound Imaging System

Start date: February 2010
Phase: N/A
Study type: Observational

This study is to collect data and learn more about the Vscan Ultrasound Imaging System. It is an "observational" study with no additional procedures or intervention prescribed other than using the Vscan along with a routine medical physical exam.

NCT ID: NCT00998218 Completed - Clinical trials for Sudden Cardiac Death

Effect of Ranolazine on Arrhythmias and Microvolt T- Wave Alternans (MVTWA) Patients With LV Dysfunction

Start date: September 2009
Phase: Phase 3
Study type: Interventional

The purpose this investigation is to more thoroughly investigate the effects of ranolazine on arrhythmias and microvolt t-wave alternans in patients who have an automatic implantable cardioverter defibrillator (AICD) implanted either prophylactically to prevent sudden cardiac death, as well as in patients who may have had a clinically significant arrhythmic event prompting the insertion of the automatic implantable cardioverter defibrillator. It is anticipated this study will provide valuable new insight into the potential use of ranolazine to treat arrhythmias in higher risk patients.