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Heart Failure clinical trials

View clinical trials related to Heart Failure.

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NCT ID: NCT02149940 Completed - Heart Failure Clinical Trials

Feasibility of Pharmaceutical Interventions in Elderly Heart Failure Patients.

RASP-HF
Start date: April 2013
Phase: N/A
Study type: Interventional

Heart failure therapies (e.g. beta blockers) have been successful in decreasing mortality rates, as well as diminishing hospitalizations. Also, pharmacist collaboration has been shown to have a beneficial impact on heart failure related outcomes. Regardless, a high residual event rate is to be noted. In our pilot study, we wished to document whether a clinical pharmacist could still play a role in the heart failure management of an elderly inpatient heart failure population.

NCT ID: NCT02149316 Completed - Heart Failure Clinical Trials

Remote Ischemic Preconditioning With Postconditioning in Heart Transplantation Surgery

Start date: February 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether remote ischemic preconditioning with postconditioning (RIPC+RIPostC) reduces myocardial injury and improves clinical outcomes in heart transplantation surgery.

NCT ID: NCT02149290 Completed - Heart Failure Clinical Trials

LifeVest Trends Validation Protocol

TRENDS
Start date: February 2014
Phase:
Study type: Observational

This study will evaluate the accuracy of data on body position, daily activity, heart rate, 6-minute walk test, and a health survey collected by the wearable cardioverter defibrillator (WCD).

NCT ID: NCT02148679 Completed - Heart Failure Clinical Trials

Geriatric Out of Hospital Randomized Meal Trial in Heart Failure

GOURMET-HF
Start date: May 2014
Phase: N/A
Study type: Interventional

Study subjects will receive either pre-prepared, home-delivered DASH/SRD-compliant meals or attention control for 4 weeks after hospital discharge.

NCT ID: NCT02148341 Completed - Heart Failure Clinical Trials

Implementation of the Hospital to Home (H2H) Heart Failure Initiative

Start date: January 2010
Phase: N/A
Study type: Interventional

This study determines if a community of practice of clinicians and quality improvement specialists can be used to implement a national quality initiative known as Hospital to Home (H2H). This quality initative is designed to reduced readmission rates for patients with heart failure or heart attack by improving the transition of care upon discharge.

NCT ID: NCT02147613 Completed - Clinical trials for Diastolic Heart Failure

High Intensity Interval Exercise in Diastolic Heart Failure

Start date: November 2010
Phase: N/A
Study type: Interventional

Heart failure is a major health concern and is the leading cause of hospitalization among elderly Americans. Currently 5.7 million Americans are estimated to have heart failure and the estimated direct and indirect costs of treating heart failure are approximately $37.2 billion. Approximately 40% of those diagnosed with heart failure will have heart failure with preserved ejection fraction (HFPEF). These individuals have significant restrictions in their ability to carry out activities of daily living. Exercise training has been established as adjuvant therapy in heart failure. Although exercise training guidelines for treatment of heart failure with reduced ejection fraction (HFREF) are well established, no consensus exercise guidelines exist for management of HFPEF. Aerobic and cardiovascular adaptations are generally greater after high-intensity exercise training; interval-type exercise facilitates this type of training because it allows for rest periods that make it possible for patients with heart failure to perform short (e.g., 1-4 minutes) work periods at intensities that are higher than would be possible during continuous exercise. High-intensity aerobic interval training presents a unique, yet untested, therapeutic modality for the exercise training of patients with heart failure with preserved ejection fraction. Pilot testing is warranted, results of which may have important implications for reducing cardiovascular risk, increasing short- and long-term quality of life and survival, and reducing healthcare costs in this patient population. The investigators primary specific aim is to determine the efficacy of a novel, high-intensity aerobic interval exercise training program for improving VO2peak (peak oxygen uptake), endothelial function, and arterial stiffness in patients with HFPEF. The investigators secondary aim is to determine whether the vascular changes are correlated with the changes in VO2peak.

NCT ID: NCT02146794 Completed - Heart Failure Clinical Trials

Renal Denervation in Chronic Heart Failure

REACH
Start date: May 2011
Phase: Phase 1
Study type: Interventional

Renal denervation can be carried out for heart failure

NCT ID: NCT02145351 Completed - Clinical trials for Heart Failure, Diastolic

Efficacy Study of Pacemakers to Treat Slow Heart Rate in Patients With Heart Failure

RAPID-HF
Start date: April 7, 2014
Phase: N/A
Study type: Interventional

Determine the impact of restoring normal heart rate response during exercise and daily activity in patients with heart failure and a preserved ejection fraction (HFpEF) and chronotropic incompetence (CI).

NCT ID: NCT02141607 Completed - Shock Clinical Trials

Evolution of Molecular Biomarkers in Acute Heart Failure Induced by Shock

Shockomics
Start date: October 2014
Phase:
Study type: Observational

The relationship between shock, ischemia and reperfusion (I/R) injury, hemodynamic instability, systemic inflammatory response syndrome and multiorgan failure has been extensively investigated, but there is no consensus on the trigger mechanisms of tissue injury at the molecular level. Current therapies are targeted to reduce symptoms of shock and multiorgan damage but they are unable to act at the "beginning of the cascade", because of the lack of a model explaining the molecular basis of shock induced tissue injury and ensuing organ damage. The present observational study is aimed at identifying the molecular triggers of acute heart failure (HF) induced by shock and to identify inflammatory mediators and markers that are activated in shock, with a particular emphasis on the role of uncontrolled proteolytic activity.

NCT ID: NCT02140905 Completed - Heart Failure Clinical Trials

Neck-Worn Monitoring Sensor for - A Study for Monitoring Subjects With Fluid-Management Issues During Dialysis

Start date: April 2014
Phase: N/A
Study type: Observational

The study has two objectives based on the intended-use measurements and populations described above. The first objective is to show that relative changes in impedance as measured by the test device (ΔSFI) are strongly correlated with the amount of fluid removed during dialysis (ΔF) for subjects with ESRD and possibly Heart Failure. The second objective is to demonstrate correlation between ΔSFI and relative changes in impedance (ΔZ) as measured by the reference device.