Clinical Trials Logo

Heart Failure clinical trials

View clinical trials related to Heart Failure.

Filter by:

NCT ID: NCT02949544 Completed - Heart Failure Clinical Trials

Water Immersion in Chronic Stable Heart Failure

IMMERSE-HF
Start date: November 22, 2016
Phase: N/A
Study type: Interventional

This study aims to investigate the effects of water immersion and exercise on heart function and blood flow in patients with chronic stable heart failure.

NCT ID: NCT02949531 Completed - Heart Failure Clinical Trials

Use of Oxygen in Heart Failure With Preserved Ejection Fraction

STOP-EF
Start date: November 3, 2016
Phase: Phase 2
Study type: Interventional

Oxygen is routinely given to patients with common conditions such as COPD and heart failure. There is no evidence behind giving oxygen to patients specifically in heart failure due to a stiff heart. This study aims to explore the effect oxygen has on the ability of patients with chronic heart failure and the ability to exercise. Other common variables will be assessed such as heart rate and blood pressure to observe the response to varying concentrations of oxygen. The concentrations chosen are commonly offered in hospitals and indeed are being delivered through standard equipment found in all hospitals in the country. It is hoped that studying the effect of short term oxygen on patients with heart failure will help to identify the effectiveness of oxygen in longer term therapy for patients who are often breathless with a decreased exercise tolerance.

NCT ID: NCT02946476 Completed - Clinical trials for Heart Failure, Systolic

Prognostic Impact of Noncardiac Comorbidities in Heart Failure Patients

NCC-HF
Start date: November 2009
Phase: N/A
Study type: Observational

To better understand the public health prognostic impact of noncardiac chronic illnesses, we explored the attributable risk of noncardiac comorbidities on outcomes between heart failure patients with reduced ejection fraction (HFREF) and heart failure patients with preserved ejection fraction (HFpEF) in a large contemporary heart failure (HF) population The adjusted hazard ratio (HR) and the population attributable risk were used to compare the contributions of 15 noncardiac comorbidities to adverse outcome. The comorbidities that contributed to high attributable risk were: anemia, chronic kidney disease, chronic obstructive pulmonary disease, diabetes mellitus, and peripheral artery disease. These findings were similar for HFrEF and HFpEF groups. Interaction analysis confirmed similar results.

NCT ID: NCT02943941 Completed - Heart Failure Clinical Trials

Pressure Variability Study

APVS
Start date: July 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to understand how the pressure in the pulmonary artery changes under different conditions of posture, respiration and exertion.

NCT ID: NCT02943590 Completed - Heart Failure Clinical Trials

STOP-CA (Statins TO Prevent the Cardiotoxicity From Anthracyclines)

Start date: January 13, 2017
Phase: Phase 2
Study type: Interventional

This research study will test whether atorvastatin, a drug commonly prescribed for reducing cholesterol levels, can protect the heart during chemotherapy with doxorubicin. Atorvastatin is from a family of medications that are commonly called "statins"

NCT ID: NCT02941705 Completed - Clinical trials for Congestive Heart Failure

Regression of Fibrosis & Reversal of Diastolic Dysfunction in HFpEF Patients Treated With Allogeneic CDCs

RegressHFpEF
Start date: July 12, 2017
Phase: Phase 2
Study type: Interventional

Perform a randomized, double blind, placebo-controlled Phase 2a feasibility study to determine whether treatment of HFpEF patients with intracoronary allogeneic CDCs affects clinical functional status (QOL scores), exercise tolerance (6MHW), exercise hemodynamics (supine exercise ergometry during right heart catheterization), myocardial interstitial fibrosis (MRI with native T1 mapping and calculation of extracellular volume [ECV] after gadolinium administration), macroscopic fibrosis by delayed gadolinium enhancement (DGE), and diastolic function (catheterization, echocardiography, BNP). Treatment of patients with symptomatic hypertensive heart disease-induced HFpEF with allogeneic CDCs will be safe and will improve clinical functional status, exercise tolerance/hemodynamics, myocardial interstitial structure, and diastolic function; the mechanisms underlying these improvements will be reflected in changes in plasma biomarkers that indicate a reduction in pro-inflammatory and pro-fibrotic signaling.

NCT ID: NCT02941315 Completed - Clinical trials for Cardiomyopathy With Unknown Etiology

Risk Stratification of Heart Failure in Cardiomyopathies.

EARLY-MYO-HF
Start date: December 1, 2016
Phase: Phase 1
Study type: Interventional

The investigators aimed to use CMR technique in helping diagnose the etiology of unknown cardiomyopathy. Try to make a risk stratification of susceptible heart failure based on the extent of myocardial impairment.

NCT ID: NCT02939157 Completed - Clinical trials for Heart Failure, Congestive

Pocket-sized Ultrasound for Point-of-care Diagnosis of Heart Failure

POCUS
Start date: December 12, 2016
Phase:
Study type: Observational

Assessment of pocket sized ultrasound (Vscan GE Healthcare) for diagnosing heart failure in primary care patients, with a comprehensive cardiac ultrasound examination (Siemens Acusan P10) performed at a specialized the eco.lab, as reference.

NCT ID: NCT02939053 Completed - Clinical trials for NYHA Class III Heart Failure

Correlation of SOZO BIS Measures With CardioMEMS PA Pressure

Start date: August 29, 2017
Phase:
Study type: Observational

This study aims to establish the degree to which change in the ratio of ECF to TBW measured using the SOZO BIS device correlates with change in end-expiratory end-diastolic PAP measured using the CardioMEMS HF System (St. Jude Medical).

NCT ID: NCT02938260 Completed - Heart Failure Clinical Trials

Diltiazem vs. Metoprolol in the Acute Management of AF in Patients With HFrEF

Start date: October 2016
Phase:
Study type: Observational

Atrial fibrillation (AF) is the most common arrhythmia, accounting for one third of all hospital admissions and 1% of all emergency department visits (ED). Approximately 65% of those presenting to the ED with AF are admitted. There are also numerous reasons for patients to get AF with rapid ventricular rate (AF RVR) during hospitalization. In the acute setting these patients are often treated with diltiazem, a non-dihydropyridine calcium channel blocker (ND CCB), or metoprolol, a beta blocker (BB). Non-dihydropyridine calcium channel blocker (diltiazem and verapamil) use is considered harmful and national guidelines recommend against use in patients with decompensated heart failure (HF). This recommendation is based on studies with long-term treatment. The purpose of this study is to assess the difference between metoprolol and diltiazem for the acute treatment of AF RVR in patients with HF with reduced ejection fraction (HFrEF).