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Heart Failure clinical trials

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NCT ID: NCT01085175 Withdrawn - Heart Failure Clinical Trials

Trial to Determine Imaging Parameters of LMI1195 in Heart Failure Patients at Low and High Risk of Defibrillator Firing

LMI1195-201
Start date: May 2010
Phase: Phase 2
Study type: Interventional

The purpose of this clinical study is to determine the optimal imaging parameters and assess the safety of LMI1195 -101 in Heart Failure subjects at Low and High Risk of cardiac events.

NCT ID: NCT01082601 Withdrawn - Atrial Fibrillation Clinical Trials

Catheter Ablation for Atrial Fibrillation and Heart Failure

Start date: April 2010
Phase: N/A
Study type: Observational

To compare heart function, symptoms, exercise capacity and quality of life in patients with Congestive Heart Failure (CHF) and Atrial Fibrillation (AF)before and after catheter ablation. Hypothesis: Restoration and maintenance of sinus rhythm by catheter ablation, without the use of antiarrhythmic drugs, in AF and CHF improves heart failure status.

NCT ID: NCT01077167 Withdrawn - Heart Failure Clinical Trials

Pharmacokinetic Study of Omecamtiv Mecarbil in Heart Failure Patients

Start date: July 2010
Phase: Phase 2
Study type: Interventional

The purpose of this trial is to obtain a pharmacokinetic profile (i.e. amount of drug in the blood over time) of Omecamtiv mecarbil in patients with stable heart failure.

NCT ID: NCT01022983 Withdrawn - Heart Failure Clinical Trials

Preoperative Levosimendan and Heart Failure

PELS
Start date: April 2011
Phase: Phase 4
Study type: Interventional

The purpose of this study is to investigate the safety and efficacy of Levosimendan given preoperative to patients with heart failure undergoing noncardiac surgery.

NCT ID: NCT01014000 Withdrawn - Heart Failure Clinical Trials

Comparative Study to Examine Whether Echocardiography Performed During Cardiac Resynchronization Therapy Device Implantation Can Improve the Response Rate

E-OPT
Start date: June 2015
Phase: N/A
Study type: Interventional

Empirical implantation of the left ventricular lead is the prevailing practice in cardiac resynchronization therapy device implantation. The response rate to the therapy has been uniformly 70% only despite various methods to screen patients before device implantation. This study tested the hypothesis that echocardiography to assess acute resynchronization of the left ventricle during device implantation may improve the response rate to the therapy.

NCT ID: NCT01007981 Withdrawn - Heart Failure Clinical Trials

A Novel Echocardiography Modality to Assess Left Ventricular Dyssynchrony

Start date: November 2008
Phase: N/A
Study type: Observational

The investigators hypothesize that the relation between mechanical and hemodynamic left ventricular dyssynchrony might better predict response to Cardiac Resynchronization Device(CRT) than currently existing echo indices.

NCT ID: NCT00922402 Withdrawn - Acute Heart Failure Clinical Trials

Heart & Diabetes - Feasibility Study

Start date: June 2009
Phase: N/A
Study type: Interventional

The main purpose of this study is to validate an intensive protocol of insulin infusion and subsequent subcutaneous insulin administration with the support of continuous glucose monitoring, in addition to reference finger-stick values.

NCT ID: NCT00906100 Withdrawn - Heart Failure Clinical Trials

Prevalence of Atrial Delay That Would Preclude Optimization of Atrioventricular (AV) Delay in Patients With Biventricular (BiV) Device

Start date: May 2008
Phase:
Study type: Observational

The purpose of this study is to determine the proportion of patients who are undergoing Biventricular (BiV) Implantable Cardioverter Defibrillator (ICD) implantation in whom optimization of atrioventricular (AV) delay is not possible due to prolonged inter-atrial/intra-atrial delay. These patients would benefit from left atrial pacing, and if a significant number of patients fall into this group, it may be beneficial to develop a left atrial lead.

NCT ID: NCT00887055 Withdrawn - Heart Failure Clinical Trials

OPTIMA Bi-ventricular Capture Verification Study

Start date: n/a
Phase: Phase 4
Study type: Observational

The purpose of this study is to characterize the morphology (shape) of the intracardiac electrograms(EGM) from patients with a resynchronization therapy device.

NCT ID: NCT00886548 Withdrawn - Heart Failure Clinical Trials

Echocardiographic Examination Performed by Nurses in Cardiac Intensive Care Unit

Start date: April 2009
Phase:
Study type: Observational

The purpose of this study is: - To study the clinical usefulness of nurse-performed ultrasound and echocardiographic examinations in a cardiac intensive care unit. - To study reproducibility of nurse-performed ultrasound and echocardiographic examinations in a cardiac intensive care unit. - To study which ultrasound measure that best correlate with the amount of pleural effusion.