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Left Ventricular Dysfunction clinical trials

View clinical trials related to Left Ventricular Dysfunction.

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NCT ID: NCT03257436 Completed - Clinical trials for Left Ventricular Dysfunction

Strategic Management to Improve CRT Using Multi-Site Pacing Post Approval Study (Reference # C1918)

SMARTMSP
Start date: January 5, 2018
Phase: N/A
Study type: Interventional

Prospective, multi-center, single arm, post approval study to be conducted in the United States.

NCT ID: NCT03232736 Completed - Heart Diseases Clinical Trials

InterventiOn of Biventricular Pacemaker Function on ventrIcular Function Among Patients With LVAD's

ROBIN
Start date: October 1, 2017
Phase:
Study type: Observational

The primary reason the investigators are doing this study are to understand how the right side of the heart functions in heart failure patients with left ventricular assist devices (LVADs, or "mechanical hearts"). Second, the investigators are interested in understanding how different pacemaker settings influence function of the heart at rest and activity.

NCT ID: NCT03107923 Completed - Clinical trials for Aortic Valve Stenosis

Better Patient Selection to Transcatheter Aortic Valve Implantation

Start date: April 26, 2017
Phase:
Study type: Observational [Patient Registry]

This study evaluates whether a preoperative assessment of myocardial contractile reserve by tissue Doppler Imaging and myocardial fibrosis by cardiac magnetic resonance imaging (MRI) can enhance the patient selection and risk stratification to transcatheter aortic valve implantation.

NCT ID: NCT02956577 Completed - Clinical trials for Left Ventricular Dysfunction

Cardiac Function and Microcirculation: Type 2 DIABetes and ECHOcardiographic Changes Over Time

DIABECHO
Start date: March 16, 2016
Phase:
Study type: Observational

The purpose of this study was to investigate the influence of micro- and macrovascular changes on the cardiac function in relation to left ventricular function and coronary arteries during one year in patients with type 2 diabetes.

NCT ID: NCT02687932 Completed - Clinical trials for Mitral Valve Insufficiency

Pharmacological Reduction of Functional, Ischemic Mitral REgurgitation

PRIME
Start date: March 2016
Phase: Phase 4
Study type: Interventional

Functional MR is caused by adverse left ventricular remodeling after myocardial injury and associated with an increased incidence of heart failure and death. Because secondary functional MR usually develops as a result of LV dysfunction, diuretics, beta blockers, angiotensin-converting-enzyme (ACE) inhibitors or angiotensin receptor blockers (ARB), and aldosterone antagonists are given to patients with functional MR in line with the guidelines in the management of heart failure. However, functional MR appears to remain common despite use of these drugs and current medical treatment is usually insufficient for reducing MR or reversing the adverse LV remodeling. As LCZ696 is a dual-acting inhibitor of the renin-angiotensin-aldosterone system (RAAS) and neutral endopeptidase (NEP), LCZ696 has greater hemodynamic and neurohormonal effects than ARB alone. Investigators try to examine the hypothesis that LCZ696 is superior to ARB alone in improving functional MR in patients with LV dysfunction and functional MR.

NCT ID: NCT02354989 Completed - Atrial Fibrillation Clinical Trials

Rate RESPONSIVe Pacing in Patients With Permanent AF Underwent AV Node ABLation and bivEntricular Pacing (RESPONSIBLE)

RESPONSIBLE
Start date: January 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effect on distance covered in a 6 minute walking test of Rate Responsive pacing in patients with permanent atrial fibrillation and reduced left ventricular ejection fraction treated with atrioventricular junction ablation and biventricular pacing.

NCT ID: NCT02013037 Completed - Clinical trials for Left Ventricular Dysfunction

The De-novo Use of Eculizumab in Presensitized Patients Receiving Cardiac Transplantation

DUET
Start date: November 2012
Phase: Phase 3
Study type: Interventional

All individuals who receive a heart transplant are at risk for developing antibody-mediated rejection (AMR). An antibody is a protein produced by the body's immune system when it detects a foreign substance, called an antigen. The mechanism of an antibody is to attack an antigen. In antibody mediated rejection, antibodies will attack the transplanted heart, causing injury to the heart. The purpose of this investigation is to determine if a study drug, called eculizumab (Soliris), is safe to use in heart transplant recipients, and determine if it reduces risk of antibody-mediated rejection.

NCT ID: NCT01971125 Completed - Clinical trials for Diabetes Mellitus, Type 2

Left Ventricular DYsfunction in DiAbetes

DYDA
Start date: July 2006
Phase:
Study type: Observational

The purpose of this study is to evaluate the prevalence, during the enrolment, of Left Ventricular Dysfunction diastolic and/or systolic in patients with diabetes mellitus type 2 without known or documented heart disease history and recognize its predictive clinical, biohumoral and with non-invasive techniques parameters.

NCT ID: NCT01609738 Completed - Heart Failure Clinical Trials

Left Ventricular Septum Pacing in Patients by Transvenous Approach Through the Inter-ventricular Septum

Start date: November 2012
Phase: Phase 1/Phase 2
Study type: Observational

Cardiac pacing is the only effective treatment for symptomatic bradycardia. The right ventricular apex (RVA) has become the most frequently used ventricular pacing site. However, RVA pacing has been shown to cause left ventricular (LV) dyssynchrony wich can lead to LV dysfunction and development of heart failure. Recent studies in animals have demonstrated that pacing at the LV septum induces significantly less ventricular dyssynchrony than RVA pacing and is able to improve LV function to a similar degree as biventricular (BiV) pacing. In addition it was shown that a LV septum lead can be placed permanently by driving a lead with extended helix from the RV side through the inter-ventricular septum into the LV endocardial layer. This was shown to be a feasible and safe procedure and lead stability was shown during four months of follow-up in otherwise healthy and active canines. LV septum pacing may therefore be a good treatment alternative in patients with symptomatic bradycardia, as well as patients with an indication for cardiac resynchronization therapy (CRT). The purpose of this study is to translate the findings from preclinical studies to the clinical situation by investigating the feasibility, long-term lead stability and safety of LV septum pacing by transvenous approach through the inter-ventricular septum in patients.

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.