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Heart Failure clinical trials

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NCT ID: NCT02378402 Completed - Myocardial Lipid Clinical Trials

Myocardial Lipid and Creatine of Heart Failure on MRS

Start date: January 2014
Phase:
Study type: Observational

The objective of this 3-year project is to develop myocardial MRS, in particular lipid (triglyceride) and creatine resonances, as imaging biomarkers for patients with heart failure (HF). Investigators will elucidate how and, to what extent, lipid and creatine levels of the heart contribute to heart failure. The first year is a cross-sectional study. Investigators aim to compare the MRS of normal subjects and that of stable HF patients in recovery with normal or impaired ejection fraction (EF). Total 60 subjects will be enrolled, with 20 subjects in each group. In the 2nd and 3rd years, investigators plan a prospective longitudinal study of 40 subjects. Enrolled patients will be evaluated with cardiac MRS at three time points, i.e., disease onset, 6 months and one year after treatment, and will be followed up until the end of this project (1.5~3-year follow up). In total 120 MR scans will be performed in the 2nd and 3rd years. The resonances from cardiac MRS, including creatine and lipids, will be correlated with the disease course, patient biochemistry data and clinical outcome. Investigators expect to make MRS to become an integral part of a clinical cardiac MR protocol.

NCT ID: NCT02372292 Completed - Clinical trials for Cardiorenal Syndrome

Value of Renal Vascular Doppler Sonography in Management of Decompensated Heart Failure

Start date: February 2013
Phase: N/A
Study type: Interventional

Although the traditional determinant of renal dysfunction in heart failure was suggested as decreased cardiac output and renal hypo perfusion, recent studies have demonstrated the association of persistent systemic venous congestion and kidney dysfunction. Relief of the congestion has demonstrated to improve renal functions in decompensated heart failure. The current trial was set up to investigate the changes of renal venous impedance and renal arteriolar resistivity indices with diuretic therapy, in patients with congestive renal failure. The investigators asked whether measurement of renal venous impedance index or renal arteriolar resistivity index can guide the practice of diuretic therapy.

NCT ID: NCT02369419 Completed - Heart Failure Clinical Trials

Frailty Score Assessment for Elderly Patients Undergoing Cardiac Resynchronization Therapy

FRAILTY
Start date: January 2013
Phase: N/A
Study type: Observational

Background: The cardiac resynchronization therapy (CRT) has been shown to improve symptoms and outcome of patients with congestive heart failure (HF), and depressed left ventricular ejection fraction (LVEF < 35 %). The rate of non-responders to CRT is estimated at 30 %. Yet, the impact of frailty on the response to CRT has not been studied, until now. Purpose : To assess the impact of frailty in the elderly, on the response to CRT.

NCT ID: NCT02369042 Completed - Clinical trials for Congestive Heart Failure(CHF)

KYMA Device: External Measure of Thoracic Fluid and Vital Signs

Ease
Start date: October 2014
Phase: N/A
Study type: Interventional

External measure of thoracic fluid content (TFC) combined with vital signs (HR,respiratory rate(RR), posture and movements) using the technology developed by Kyma Medical Technologies while tracking clinical changes in acute in-hospital and chronic outpatient heart failure patients.

NCT ID: NCT02368548 Completed - Heart Failure Clinical Trials

Randomized Clinical Trial of a Pharmaceutical Care Program in Chronic Patients Users of an Emergency Department

Start date: January 2012
Phase: N/A
Study type: Interventional

The study aims to assess the clinical and economic impact of a pharmaceutical care program initiated in the Emergency Department versus conventional follow-up of patients with decompensated heart failure/COPD.

NCT ID: NCT02367716 Completed - Clinical trials for Chronic Heart Failure

Post-market Study of Multi-Vector Left Ventricular Lead Performance in Chinese Patients With Chronic Heart Failure

MVLV
Start date: December 2014
Phase:
Study type: Observational

The purpose of this clinical study is to observe the safety and efficacy of the multi-vector left ventricular (LV) lead in Chinese patients that are indicated for Cardiac Resynchronization Therapy (CRT).

NCT ID: NCT02362646 Completed - Heart Failure Clinical Trials

Safety & Efficacy of Intramyocardial Injection of Mesenchymal Precursor Cells on Myocardial Function in LVAD Recipients

Start date: July 2015
Phase: Phase 2
Study type: Interventional

The main purpose of this research is to determine whether injecting mesenchymal precursor cells (MPC) into the heart during surgery to implant a left ventricular assist device (LVAD) is safe. MPCs are normally present in human bone marrow and have been shown to increase the development of blood vessels and new heart muscle cells in the heart. In addition, this research is being done to test whether injecting the MPCs into the heart is effective in improving heart function.

NCT ID: NCT02359227 Completed - Heart Failure Clinical Trials

Safety Study of Cenderitide in Stable Chronic Heart Failure

Start date: January 2015
Phase: Phase 2
Study type: Interventional

Planned enrollment is approximately twelve subjects with stable chronic heart failure. Enrolled subjects will receive up to eight sequential days of continuous, stepwise, dose increasing, subcutaneous (SQ) infusions of open-label cenderitide via the Insulet Drug Delivery System. Planned infusion rates of cenderitide will be administered to subjects continuously during four, 48-hour infusion periods.

NCT ID: NCT02358525 Completed - Heart Failure Clinical Trials

Effects of a Rehabilitation Program on Immune Activation and Mood in Heart Failure Patients

Start date: January 2015
Phase: N/A
Study type: Observational

The aim of this descriptive study is to examine potential changes regarding inflammatory cytokine levels, depressive symptoms and quality of life over the course of the 4-week inpatient rehabilitation program which includes a cassette of modalities including counseling, psychosocial education and supervised exercise training as a main pillar, and to further investigate if there are correlations between changes in immune regulation, depressive symptoms and quality of life.

NCT ID: NCT02356393 Completed - Clinical trials for Myocardial Infarction

Serum Magnesium Levels in Desalination Tap Water and Outcomes in Acute Myocardial Infarction Patients

Start date: May 2015
Phase:
Study type: Observational

Association between serum magnesium and clinical outcome in patients with acute MI (AMI) with 1 year follow-up in 300 patients in regions supplied by desalinated drinking water (DSW) (Sheba MC) and 150 patients in regions with non-desalinated drinking water (DW) (Nahariya MC).