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Cardiomyopathies clinical trials

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NCT ID: NCT02855554 Recruiting - Clinical trials for Cardiomyopathy, Myocarditis, Ischemic Heart Disease

Quantitative Cardiac Parametric Mapping

Myomapping
Start date: June 20, 2014
Phase: N/A
Study type: Interventional

The overall goal of this project is to evaluate the clinical potential of fast quantitative myocardial tissue characterization using recently emerged Cardiac Magnetic Resonance Imaging (CMR) techniques to aid the diagnosis, treatment, and follow up of patients with myocardial diseases, such as ischemic heart disease, cardiomyopathies, and myocarditis.

NCT ID: NCT02824822 Recruiting - Epilepsy Clinical Trials

Genetic Markers of Cardiovascular Disease in Epilepsy

Start date: May 2016
Phase:
Study type: Observational

Epilepsy is a common condition which affects over 3 million people in the US. Patients with uncontrolled epilepsy have a lifetime risk of sudden unexpected death (SUDEP) of 35%, which is greatest in those under 40 years of age. The exact mechanisms and causes are not understood but can be due to underlying conditions which affect the heart and brain, which may lead to dangerous heart rhythms and death. Some of these conditions which affect heart and brain have an identifiable genetic cause. This study aims to identify known genetic causes of heart rhythm and sudden death related disorders in patients with epilepsy.

NCT ID: NCT02804269 Recruiting - Healthy Clinical Trials

Molecular and Imaging Studies of Cardiovascular Health and Disease

Biobank
Start date: July 2013
Phase: N/A
Study type: Observational

Biobank is a program which collects biological samples, health information and imaging data from consented patients and stored them at the core facility. These information would be used to study the molecular, imaging and outcome studies of cardiovascular health and disease.

NCT ID: NCT02804256 Recruiting - Clinical trials for Ischemic Heart Disease

Biomarkers of Inherited Cardiovascular Conditions

Start date: January 2014
Phase: N/A
Study type: Observational

The National Heart Centre Singapore has recently created a biorepository that is IRB approved for the use in genetic studies: "molecular and imaging studies of cardiovascular health and disease (CIRB Ref: 2013/605/C)". This repository enables IRB approved projects within the National Heart Centre Singapore to access the samples for use in biomarker or genetic studies with consent from patients for these studies. The IRB approved biorepository process also allows for patients, when they have consented to this, to be approached for inclusion in additional studies at National Heart Centre Singapore. In this study, the investigators will examine the genetic variation in genes known to cause inherited cardiac conditions and also look for circulating biomarkers (ICC) in 600 patients with ICC and in 500 patients with ischemic heart disease (e.g.IHD) who will be used as controls. Healthy controls will also be used (800) as they become available in the biorepository. All samples have already been collected in the NHCS biorepository. These patients would have been recruited and consented to the biorepository. This will enable all to better understand heart disease in Singaporean patients. In addition, the investigators will invite a subset of 10 patients with ICCs to provide a second blood sample (20mls - 2 tablespoons) on top of the samples that will be collected for the biorepository. The second blood sample will be used for antibody biomarkers that will be developed in the basic science laboratories. These antibodies will be used to develop new biomarkers of human heart disease to improve human health.

NCT ID: NCT02735811 Recruiting - Cardiomyopathies Clinical Trials

OBSERVational Registry on Long-term Outcome of ICD Patients

OBSERVO
Start date: March 2015
Phase: N/A
Study type: Observational

Multicentric, observational, retrospective registry including patients underwent ICD implantation for any indication. The primary aim of the registry is to evaluate the long-term outcome of patients receiving an ICD.

NCT ID: NCT02696135 Recruiting - Clinical trials for Cardiomyopathy, Hypertrophic

The Chinese Hypertrophic Cardiomyopathy Study(CHCS)

CHCS
Start date: March 23, 2011
Phase:
Study type: Observational

Hypertrophic cardiomyopathy (HCM) is one of the most common inherited cardiac diseases, with a prevalence of ∼0.2%. Sudden cardiac death (SCD), heart failure and stroke are the major poor outcomes of HCM. Although about half of the patients were found to be caused by mutations mainly located in genes encoding sarcomere proteins, the causes in a significant proportion of patients with HCM are still unknown. Even in the patients with sarcomere mutations, the molecular pathways that eventually lead to cardiac hypertrophy are remained to be revealed. Furthermore, HCM presents with significant heterogeneity. SCD risk stratification and prevention by ICD are necessary. However, the strategy of SCD risk stratification recommended by the 2011 ACCF/AHA and 2014 ESC guidelines were based mainly on the evidence derived from American and European countries. The accuracy of these guidelines in Chines patients with HCM was not evaluated yet.

NCT ID: NCT02692508 Recruiting - Cardiomyopathy Clinical Trials

Prognosis of Subjects With Unexplainable Precordial Deep T-wave Inversion Without Wall Thickness> 15mm

Start date: January 2011
Phase: N/A
Study type: Observational

The investigators sought to evaluate the morphological and functional changes and prognosis of participants with unexplainable precordial deep T-wave inversion on ECG and with apical thickness less than 15mm. The conduction of this study was largely due to the increased clinical requirement, which reflected the increased awareness among physicians of missed AHCM.

NCT ID: NCT02681913 Recruiting - Cardiomyopathies Clinical Trials

Adenosine as an Adjunct to Blood Cardioplegia

Start date: February 2016
Phase: Phase 2
Study type: Interventional

Myocardial protection is a major issue in cardiac surgery, since inadequate protection increases the risk of postoperative cardiac dysfunction. The main principle of myocardial protection in cardiac surgery is to preserve myocardial function by preventing ischemia with blood cardioplegia . Previous studies have shown that adenosine as an adjunct to blood cardioplegia can be safely used in cardiac surgery. In the Amphia Hospital, adenosine is already used as standard care as an initial cardioplegic bolus in minimally invasive port access operations. Whether, adenosine as an adjunct to intermittent warm blood cardioplegia, has an added value remains unclear. Therefore the investigators would like to investigate the effect of the addition of adenosine to standard intermittent warm blood cardioplegia in patients scheduled for minimally invasive, port access operations (mitral valve surgery). Half of the participants will receive standard intermittent warm blood cardioplegia, while the other half will receive intermittent warm blood cardioplegia enriched with adenosine.

NCT ID: NCT02641145 Recruiting - Cardiomyopathy Clinical Trials

Molecular Imaging of Primary Amyloid Cardiomyopathy

MICA
Start date: April 1, 2016
Phase: N/A
Study type: Interventional

Cardiac amyloidosis is a major cause of early treatment-related death and poor overall survival in individuals with systemic light chain amyloidosis. This project will develop a novel approach to visualize cardiac amyloid deposits using advanced imaging methods. The long-term goal of this work is to identify the mechanisms of cardiac dysfunction, in order to guide the development of novel life-saving treatments.

NCT ID: NCT02601066 Recruiting - Clinical trials for Cardiomyopathy Associated With Myopathy and Sudden Death

Cardiac Arrhythmias and Sudden Death in Patients Affected With Laminopathies

Start date: September 2015
Phase: N/A
Study type: Interventional

This research study includes patients ages 1 to 25 years old with Lamin A/C related muscular dystrophy (LMNA-MD). The goal of this study is to evaluate how the heart is affected in children and teens with LMNA-MD. The evaluation includes an echocardiogram, an electrocardiogram, an electrophysiological study and the implantation of a subcutaneous ECG holter monitor.