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Dilated Cardiomyopathy clinical trials

View clinical trials related to Dilated Cardiomyopathy.

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NCT ID: NCT03062956 Completed - Clinical trials for Dilated Cardiomyopathy

A Single Ascending Dose Study Assessing the Safety, Tolerability, PK and PD of MYK-491

Start date: January 16, 2017
Phase: Phase 1
Study type: Interventional

Up to 72 healthy volunteers will be given a single dose of MYK-491 or placebo and be monitored for safety and tolerability over a 7 day period.

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.

NCT ID: NCT03057002 Recruiting - Clinical trials for Duchenne Muscular Dystrophy

UTSW HP [13-C] Pyruvate Injection in HCM

HPHCM
Start date: May 1, 2018
Phase:
Study type: Observational

The study objective is to identify the earliest changes in energy substrate metabolism in patients with cardiomyopathies (CMP). To achieve this objective, we plan first to test the hypothesis that patients with CMP present focal alterations in myocardial hyperpolarized [1-13C]pyruvate flux.

NCT ID: NCT02989181 Recruiting - Clinical trials for Obstructive Sleep Apnea

Continues Positive Airway Pressure Treatment for Patients With Dilated Cardiomyopathy and Obstructive Sleep Apnea

RIDA
Start date: November 2014
Phase: Phase 3
Study type: Interventional

The aim of this randomized controlled study is to investigate the effect of continues positive airway pressure (CPAP) treatment in patients with dilated cardiomyopathy (DCM) and concomitant obstructive sleep apnea (OSA). The primary endpoint is left ventricular function measured by magnetic resonance (improvement of at least 4%) after six months treatment with CPAP. The secondary endpoints include diastolic dysfunction, cardiovascular biomarkers and quality of life.

NCT ID: NCT02915718 Recruiting - Clinical trials for Dilated Cardiomyopathy

A Clinical Study of Immunoadsorption Therapy for Dilated Cardiomyopathy

Start date: October 2016
Phase: N/A
Study type: Interventional

Dilated cardiomyopathy (DCM) causes significant morbidity and mortality and is the third most common cause of heart failure and the most frequent reason for heart transplantation. The etiology of dilated cardiomyopathy(DCM) is complex. There is a growing body of literature suggesting that the humoral immune system activation and autoantibodies against myocardial generation play an important role in the progression of DCM. At present immunoadsorption technology has been successfully applied in autoimmune antibody removal treatment of a variety of diseases. And some applications of immunoadsorption(IA) in patients with DCM showed that immunoadsorption(IA) can indeed reduce the autoantibodies, improve symptoms and prognosis, but additional research is needed to identify indications and instruments for the IA treatment of DCM.

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: NCT02770443 Terminated - Clinical trials for Dilated Cardiomyopathy

Withdrawal of Medication in Recovered DCM

WrecEF
Start date: February 19, 2016
Phase: N/A
Study type: Interventional

Randomized study of medication withdrawal in patients who have recovered LV function in Dilated Cardiomyopathy.

NCT ID: NCT02654678 Not yet recruiting - Heart Failure Clinical Trials

Follow-up Safety Trial in Children With Chronic Heart Failure Therapy Receiving Orodispersible Minitablets of Enalapril

LENA-WP10
Start date: March 2016
Phase: Phase 2/Phase 3
Study type: Interventional

Paediatric long-term safety follow-up clinical trial in maximum 100 children with heart failure due to dilated cardiomyopathy or congenital heart disease, from 1 day to less than 12 years of age at recruitment into the preceding short-term pharmacokinetic (PK)/pharmacodynamic (PD) trials. Pharmacodynamic measurements and renal monitoring in all children after 1 , 4, 7 and 10 months of follow-up; in addition PK assessments as well as acceptability and palatability assessments in children still under enalapril Orodispersible Minitablet (ODMT) treatment.

NCT ID: NCT02652728 Not yet recruiting - Heart Failure Clinical Trials

Orodispersible Minitablets of Enalapril in Children With Heart Failure Due to Dilated Cardiomyopathy

LENA-WP08
Start date: January 2016
Phase: Phase 2/Phase 3
Study type: Interventional

Paediatric clinical trial in 50 children, from 1 month to less than 12 years of age, suffering from heart failure due to dilated cardiomyopathy, to obtain paediatric pharmacokinetic and pharmacodynamic data of enalapril and its active metabolite enalaprilat while treated for 8 weeks with enalapril in form of Orodispersible Minitablets (ODMTs), to describe the dose exposure in this patient population.

NCT ID: NCT02619825 Completed - Clinical trials for Hypertrophic Cardiomyopathy

Non-Invasive Evaluation of Myocardial Stiffness by Elastography in Pediatric Cardiology (Elasto-Pédiatrie)

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

First, investigators must determine the physiological standards across age classes of myocardial stiffness estimated by Elastography in ultrafast (estimated right ventricular stiffness [VD] and left ventricular [LV]). This will be done in groups of children without heart condition, age group (10 children per group, four age groups [0-1mois, 1 month-1 year 1 year-5 years, 5 years-15years]). Secondly, investigators will evaluate myocardial stiffness Elastography (RV and LV) on different groups of children (same age group) with cardiomyopathy and examine correlations with the conventional parameters of systolic and diastolic function of both ventricles and with myocardial strain values. The total population of the study will be 120 children (40 healthy, 80 patients).