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Heart Failure clinical trials

View clinical trials related to Heart Failure.

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NCT ID: NCT03650205 Recruiting - Heart Failure Clinical Trials

Ivabradine to Prevent Anthracycline-induced Cardiotoxicity

IPAC
Start date: January 22, 2019
Phase: N/A
Study type: Interventional

Anthracyclines are associated with cardiotoxic effects. Previous studies suggest that enalapril, and or carvedilol, protect against cardiovascular effects of these drugs. Ivabradine selectively reduces heart rate through inhibition of the cardiac pace maker IF channel, thus prolonging the duration of spontaneous depolarization in the sinus node. Additionally, ivabradine might preserve myocardial perfusion without negative inotropic effect and probably maintain cardiac contractility despite the reduction of heart rate. Ivabradine has been shown to improve outcome in patients with heart failure and angina. The aim of this study is to evaluate whether ivabradine might prevent anthracycline-induced cardiotoxicity.

NCT ID: NCT03648736 Recruiting - Clinical trials for Cardiac Insufficiency

Time Course of Circulating Myocardial Biomarkers After a TASH Procedure.

TASH
Start date: October 10, 2018
Phase:
Study type: Observational [Patient Registry]

The study evaluates the released myocardial substances in blood of HOCM patients after TASH procedure (small "controlled" myocardial infarction). This helps to identify new pathomechanisms and biomarker and thus provides a better understanding of development and progress of cardiac insufficiency.

NCT ID: NCT03644446 Recruiting - Clinical trials for Heart Failure With Reduced Ejection Fraction

Bisoprolol Plasma Residual Concentrations in Chronic Heart Failure

PREVALENT
Start date: November 2, 2017
Phase:
Study type: Observational [Patient Registry]

This study evaluate the dosage of bisoprolol plasma residual concentrations in chronic heart failure with mild to reduced ejection fraction adult patients by dose and renal function.

NCT ID: NCT03640000 Recruiting - Clinical trials for Heart Failure, Systolic

Acute Changes in Bioimpedance During Cardiac Resynchronization Therapy

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

This study aims at Optimizing measured parameters to reflect underlying pathology in dyssynchronous hearts. This is an experimental study in patients were bioimpedance measurements are performed during implantation.

NCT ID: NCT03629340 Recruiting - Heart Failure Clinical Trials

Metformin for Pulmonary Hypertension HFpEF

PH-HFpEF
Start date: February 26, 2019
Phase: Phase 2
Study type: Interventional

The main objective of this study is to determine the clinical efficacy of metformin versus placebo and the therapeutic response with regards to functional capacity and hemodynamics in PH-HFpEF.

NCT ID: NCT03628443 Recruiting - Heart Failure Clinical Trials

Cardiorenal Risk Stratification Pilot Study

CRiSPS
Start date: July 19, 2018
Phase:
Study type: Observational

This is prospective cohort study with the purpose of improving our understanding of morbidity and mortality risk in patients with heart failure and chronic kidney disease.

NCT ID: NCT03621618 Recruiting - Sepsis Clinical Trials

Clinical Assessment of Arterial Dynamic Elastance in ICU Patients, Dependent on Inotropic or Vasopressor Drugs.

Start date: March 31, 2019
Phase: N/A
Study type: Interventional

The primary goal of the study is to determine Eadyn ( = PPV/SVV) as a functional measure of arterial load, in conjunction with other actual afterload indices, systemic vascular resistance and arterial elastance. A secondary aim is the assessment of the influences of vasopressors and inotropic drugs on Eadyn, as a parameter of ventriculo-arterial coupling.

NCT ID: NCT03620526 Recruiting - Clinical trials for Heart Failure With Normal Ejection Fraction

Inhaled Iloprost and Exercise Hemodynamics and Ventricular Performance in Heart Failure With Preserved Ejection Fraction

ILO-HOPE
Start date: November 29, 2017
Phase: Phase 4
Study type: Interventional

BACKGROUND There is no effective medical treatment for heart failure with preserved ejection fraction (HFpEF). Increases in pulmonary capillary wedge pressure (PCWP) develop in patients with HFpEF. Prostacyclin analogo can possible reduced PA pressure along with PWCP pressure, as with exercise. OBJECTIVES This study try to determine whether inhlalation of iloprost improves exercise hemodynamics and cardiac reserve in HFpEF. METHODS In a double-blind, randomized, placebo-controlled, parallel-group trial, subjects with HFpEF underwent invasive cardiac catheterization with simultaneous expired gas analysis at rest and during exercise, before and 15 min after treatment with either inhaled iloprost or matching placebo.

NCT ID: NCT03615157 Recruiting - Clinical trials for Chronic Heart Failure

Effects of a Home-based Exercise Program on Functional Capacity and Quality of Life in Heart Failure Patients

Start date: January 15, 2018
Phase: N/A
Study type: Interventional

Heart failure (HF) is a multisystemic disease leading to exercise intolerance and fatigue. Supervised physical training improves functional capacity, quality of life and reduces hospital admissions in HF patients. In this way, home physical training may be a good alternative to patients who, for any reason, cannot perform supervised training. Objective: To asses the effects of a home-based training program on functional capacity, sedentary lifestyle and quality of life of patients with chronic HF compared to supervised training.

NCT ID: NCT03608085 Recruiting - Heart Failure Clinical Trials

Community Pharmacy Medication Therapy Management for Heart Failure

Start date: May 23, 2018
Phase: N/A
Study type: Interventional

Pharmacist-provided medication therapy management (MTM) services have been suggested as a way to improve heart failure (HF) outcomes and counter fragmented care. Nevertheless, broad implementation of MTM services, especially for HF, has not occurred. Therefore, the investigators propose a community engagement pilot study to evaluate the feasibility of 1) training of community pharmacists to perform MTM for HF patients by the University of Rhode Island (URI) Faculty and Brown University Physicians, 2) community pharmacists performing MTM post-training for patients discharged with HF in their own community, 3) establishment of a community based research network (CBRN) and registry to assess the efficacy of the training and the MTM intervention through collaboration among patients with HF, community pharmacists and URI pharmacists and Brown University physicians.