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Cardiomyopathies clinical trials

View clinical trials related to Cardiomyopathies.

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NCT ID: NCT03209843 Completed - Clinical trials for Ischemic Cardiomyopathy

Post-stenting Assessment of Reendothelialization With OFDI After CTO Procedure (PERFECTO)

PERFECTO
Start date: March 7, 2018
Phase: N/A
Study type: Interventional

The objective of PERFECTO is to assess the reendothelialization at 3 months after successfully CTO percutaneous intervention (PCI) with new generation drug eluting stent (DES) by OFDI analysis. Designed as a multicentric, observational and prospective study which will be conducted at University Hospital of Poitiers (France), a systematic OFDI analysis will be realized immediately after CTO-PCI and at 3 months. Known as major predictive factors of stent thrombosis, percentages of malapposition, uncovered struts and neointimal hyperplasia proliferation will be measured over the entire length of each stent implanted combining in a composite primary endpoint.

NCT ID: NCT03206294 Completed - Clinical trials for Cardiomyopathy, Diabetic

Impact of Pharmacist in Cardiology Service

Start date: March 8, 2017
Phase: N/A
Study type: Interventional

The coverage of the diabetes is a multidisciplinary care, with practitioners' implication(hospital and liberal), and other medical and paramedical profession: doctor, pharmacist, male nurse, nutritionist, etc. In fact there is a real importance of link between hospital and general medecine outside. That's why the pharmacist's presence during the hospitalization seems to be a good alternative to make the link between hospital and the outside pharmacist where patient take his treatment. Hospital pharmacis proceed to a treatment conciliation at the entrance and at discharge. By this conciliation the aim of the study is to show and quantify the impact of pharmacist presence on therapeutic target .

NCT ID: NCT03177018 Completed - Clinical trials for Arrhythmogenic Right Ventricular Cardiomyopathy

DNA Analysis From Isolated Cardiomyocytes in the Molecular Diagnosis of Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia

FA2CM-DVDA
Start date: September 13, 2016
Phase: N/A
Study type: Interventional

The main objective of this study is to assess if it is possible, at the end of endocardial voltage mapping, to accurately collect intact cardiomyocytes and to isolate high quality DNA allowing molecular testing of selected genes involved in arrhythmogenic right ventricular cardiomyopathy/dysplasia.

NCT ID: NCT03129568 Completed - Clinical trials for Dilated Cardiomyopathy

Transcoronary Infusion of Cardiac Progenitor Cells in Pediatric Dilated Cardiomyopathy

TICAP-DCM
Start date: April 14, 2017
Phase: Phase 1
Study type: Interventional

A phase 1 prospective study to determine the procedural feasibility and safety and preliminary efficacy of intracoronary infusion of cardiosphere-derived cells (CDCs) in patients with dilated cardiomyopathy.

NCT ID: NCT03092843 Completed - Clinical trials for Hypertrophic Cardiomyopathy

Functional Capacity and Quality of Life Following Septal Myectomy in Patients With HCM

SPIRIT-HCM
Start date: March 20, 2017
Phase:
Study type: Observational

Investigators aim to assess changes in exercise capacity and quality of life after septal myectomy in patient with hypertrophic cardiomyopathy.

NCT ID: NCT03090425 Completed - Clinical trials for Non Ischemic Cardiomyopathy

Inflammatory/Familial Dilated Cardiomyopathy: Is There a Link to Autoimmune Diseases? TP9a

Ikarius
Start date: June 2016
Phase:
Study type: Observational

In a hitherto ill-defined proportion of patients with inflammatory/familial cardiomyopathy, the phenotype dilative cardiomyopathy (DCM) is assumed to be the endstage of a multifactorial etiopathogenetic pathophysiology. Precipitating factors include enhanced autoimmunity, predisposition for viral infections, environmental factors in addition to a specific 'genetic background' of the individual patient. It is unresolved, whether the susceptibility to immunologically mediated myocardial damage reflects the presence of genetic risk factors shared by other autoimmune diseases, or is cardio-specific with individual predisposing factors. Aims of the project are the search for a genetic link or oredisposition to autoimmune diseases in patients with familial / inflammatory DCM.

NCT ID: NCT03081949 Completed - Clinical trials for Peripartum Cardiomyopathy

Peripartum Cardiomyopathy in Nigeria Registry

PEACE
Start date: June 12, 2017
Phase: Phase 4
Study type: Interventional

Peripartum cardiomyopathy (PPCM) is a global disease with significant morbidity and mortality, and Nigeria probably has the highest burden of the disease in the world. Unfortunately, much about the disease including its aetiology, epidemiology and treatment is not yet well described. This will be a prospective, national, multicenter cohort study, conducted in centres in Nigeria. It is expected that approximately 500 patients with PPCM and 500 apparently healthy pregnant women will be recruited over a 6-month period with follow-up at 3-monthly intervals for 18 months.

NCT ID: NCT03078881 Completed - Clinical trials for Crigler-Najjar Syndrome

Clinical Assessment Study in Crigler-Najjar Syndrome

LUSTRO
Start date: March 10, 2017
Phase:
Study type: Observational

This is a Pre-Phase 1 prospective, non-interventional clinical assessment study to evaluate Crigler-Najjar syndrome subjects requiring daily phototherapy, aged 1 year and older.

NCT ID: NCT03071835 Completed - Heart Diseases Clinical Trials

A Comparative Study of Subjects Past Their Final Follow-ON Visit

HYPERION
Start date: June 23, 2016
Phase:
Study type: Observational

A comparative study to follow subjects who received stem cell therapies three, five, seven, nine, and thirteen years after their follow-on visit. Subjects will be selected from a pool of previous Interdisciplinary Stem Cell Institute trial participants.

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.