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Hypertrophic Cardiomyopathy clinical trials

View clinical trials related to Hypertrophic Cardiomyopathy.

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NCT ID: NCT03846297 Recruiting - Clinical trials for Hypertrophic Cardiomyopathy

Optimisation of Decision Making for Defibrillator Implantation in Hypertrophic Cardiomyopathy

OPTIM-HCM
Start date: September 23, 2020
Phase:
Study type: Observational

The main objective of the study is to improve implantable cardioverter defibrillator (ICD) implantation decision-making processing relevance by developing a new prediction model of sudden cardiac death (SCD) in hypertrophic cardiomyopathy (HCM), including newly identified potential biomarkers by magnetic resonance imaging (MRI) and genetics, through a prospective nationwide study, multivariate analysis and modelling of an absolute risk. The secondary objective is to perform a medico-economic analysis of ICD implantation in order to define an optimal rule for ICD implantation in patients with HCM, taking into account the benefits of ICD, adverse effects of ICD and associated costs (cost of quality adjusted life years saved).

NCT ID: NCT03726424 Recruiting - Clinical trials for Hypertrophic Cardiomyopathy

Outcome of Different Pathogenic Mutations in Hypertrophic Cardiomyopathy

Start date: February 25, 2011
Phase:
Study type: Observational

This is a prospective, single-center study to assess clinical phenotype and prognosis of different pathogenic mutations in Chinese patients with hypertrophic cardiomyopathy. Patients with hypertrophic cardiomyopathy were consecutively recruited, and then DNA samples were extracted from peripheral blood. Targeted sequencing of 142 genes was performed to obtain variants associated with hypertrophic cardiomyopathy. Patients will undergo face-to-face interviews, phone calls, or/and chart reviews at 6 months, 12 months, 24 months, 36 months, 48 months and 60 months for data collection of clinical outcomes.

NCT ID: NCT03572569 Recruiting - Clinical trials for Hypertrophic Cardiomyopathy

Risk Stratification in Children and Adolescents With Primary Cardiomyopathy

RIKADA
Start date: January 2013
Phase:
Study type: Observational

RIKADA is a prospective study performing systematic family screening including clinical and genetic testing in pediatric patients with primary cardiomyopathy and their first-degree relatives with the aim to facilitate risk stratification.

NCT ID: NCT03362164 Recruiting - Fabry Disease Clinical Trials

Evaluation of HEArt invoLvement in Patients With FABRY Disease

HEAL-FABRY
Start date: January 2001
Phase:
Study type: Observational

This study evaluates predictors for the incidence of arrhythmias and sudden cardiac death as well as terminal heart failure in patients with Fabry disease.

NCT ID: NCT03327623 Recruiting - Clinical trials for Hypertrophic Cardiomyopathy

Sleep Apnea and Hypertrophic Cardiomyopathy (HCM)

Start date: November 13, 2017
Phase:
Study type: Observational

The investigators are trying to find out how common sleep apnea is in hypertrophic cardiomyopathy. The purpose of this study is to see if sleep apnea is common in hypertrophic cardiomyopathy and if its presence is associated with changes in the functioning of the body. The investigators want to determine if sleep apnea is associated with electrical disorders of the heart in patients with hypertrophic cardiomyopathy.

NCT ID: NCT03278457 Recruiting - Clinical trials for Hypertrophic Cardiomyopathy

Risk Stratification Using PET in HCM

HCM-PET
Start date: May 3, 2017
Phase: N/A
Study type: Observational

The overall rationale is to reduce the risk of sudden cardiac death in individuals with hypertrophic cardiomyopathy (HCM). The novel approach of this study is to correlate Positron Emission Tomography (PET) findings to ventricular arrhythmias detected by the implantable cardioverter defibrillator (ICD). This could potentially lead to an improved risk stratification of HCM patients.

NCT ID: NCT03259113 Recruiting - Clinical trials for Hypertrophic Cardiomyopathy

Insertable Cardiac Monitors in Hypertrophic Cardiomyopathy

ElucidateHcm
Start date: August 16, 2017
Phase: N/A
Study type: Interventional

Hypertrophic cardiomyopathy (HCM) is associated with sudden cardiac death and an increased risk of atrial fibrillation and subsequent embolic event. An insertable cardiac monitor will provide data on cardiac rhythm over a period of 18 months. This will provide an extended monitoring far longer than 24-48 hours of Holter monitoring as is currently usual care. Therefore, detection of arrhythmias could be used in risk stratification and decision-making with regard to offer an implantable defibrillator and anticoagulants.

NCT ID: NCT03150342 Recruiting - Clinical trials for Hypertrophic Cardiomyopathy

Presentations of Hypertrophic Cardiomyopathy on Myocardial Perfusion Imaging

Start date: May 8, 2017
Phase: N/A
Study type: Observational

Chest pain and myocardial ischemia are prevailing features in patients with hypertrophic cardiomyopathy (HCM). Recently introduced single-photon emission computed tomography (SPECT) cameras with solid-state cadmium-zinc-telluride (CZT) detectors have been shown to decrease imaging time and improved the imaging quality of gated myocardial perfusion imaging (MPI). The investigators also correlate the MPI parameters with echocardiographic parameters. This study is to examine the spatial distribution of stress perfusion abnormalities and tissue injury in patients with HCM using a CZT SPECT camera.

NCT ID: NCT03076580 Recruiting - Clinical trials for Hypertrophic Cardiomyopathy

An Integrative-"Omics" Study of Cardiomyopathy Patients for Diagnosis and Prognosis in China

AOCC
Start date: July 1, 2015
Phase:
Study type: Observational

This is a multi-omics research of Chinese cardiomyopathies patients, aiming to determine genetic risk factor and serial biomarkers of cardiomyopathies in diagnosis and prognosis.

NCT ID: NCT03061994 Recruiting - Clinical trials for Hypertrophic Cardiomyopathy

Metabolomic Study of All-age Cardiomyopathy

MAC
Start date: October 2016
Phase: N/A
Study type: Observational

This study aims to 1)characterize the differentially expressed metabolites between cardiomyopathy patients and healthy controls,2)identify the specific biomarkers associated with outcomes or risk evaluation in patients with different cardiomyopathies in a follow-up of a cohort and 3)to determine whether differentially expressed may affect the pathological process of cardiomyopathies . Standardized protocols will be used for the assessment of medical history and examinations, laboratory biomarkers, and the collection of blood plasma.