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Congestive Heart Failure clinical trials

View clinical trials related to Congestive Heart Failure.

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NCT ID: NCT02252757 Completed - Clinical trials for Congestive Heart Failure

Assess Measurements of Wireless Cardiac Output Device

Remote-CO-1
Start date: September 2014
Phase: N/A
Study type: Observational

Heart failure is a common cardiovascular problem which is increasing in both prevalence and incidence and associated with substantial morbidity and mortality. The management of heart failure patients is complex and has become a priority world over. Effective methods to keep heart failure patients out of the hospital are essential, both in the interests of the patient's health, as well as to reduce the burden on the health care system

NCT ID: NCT02191735 Completed - Heart Failure Clinical Trials

RAMP 200 / RAMP Cardiovascular Tests at the Point-of-Care

C-POC
Start date: July 2014
Phase: N/A
Study type: Observational

This clinical investigation is designed to demonstrate the performance characteristics of the RAMP® cardiac tests analyzed on the RAMP® 200 by non-laboratorial Operators at the point-of-care when compared to the results for the same samples analyzed on the RAMP® Reader.

NCT ID: NCT02173028 Completed - Clinical trials for Congestive Heart Failure

RESynchronizaTiOn theRapy and bEta-blocker Titration

RESTORE
Start date: June 2013
Phase: N/A
Study type: Observational

Patients will be treated according to the clinical practice of the participating centers and to the international guidelines for the treatment of heart failure.The present analysis provides a collection of data about the changes to drug therapy after the "Cardiac Resynchronization Therapy" (CRT) procedure , and any signs and symptoms of intolerance to prescribed medications.

NCT ID: NCT02126241 Completed - Clinical trials for Congestive Heart Failure

Non-Invasive Cardiac Output Measurement for CRT Optimization

NICaS-CRT
Start date: April 2014
Phase: N/A
Study type: Interventional

This proposal aims to evaluate the added clinical and echocardiographic benefit of using the non-invasive impedance-based cardiac output measurement system (NICaS) for optimizing atrio-ventricular and inter-ventricular delays in chronic (more than 6 months) CRT recipients.

NCT ID: NCT02120014 Completed - Clinical trials for Congestive Heart Failure

Blood Volume and Hemodynamic Analysis in Patients With Chronic Heart Failure

Start date: April 21, 2014
Phase: N/A
Study type: Interventional

The primary hypothesis is that patients with HFREF (heart failure with reduced ejection fraction) will demonstrate a markedly expanded intravascular volume which will correlate with elevated right heart hemodynamics and increased venous capacitance parameters, whereas patients with HFPEF(heart failure with preserved ejection fraction) will demonstrate euvolemia to mild volume expansion and a lack of correlation with hemodynamic and venous compliance parameters.

NCT ID: NCT02105207 Completed - Clinical trials for Congestive Heart Failure

Comparison Between Lung Ultrasound and Chest Radiography for Acute Dyspnea

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

For patients presenting to the Emergency Department with acute dyspnea, emergency physicians will be asked to categorize the diagnosis as acute decompensated heart failure or non-cardiogenic shortness of breath a) after the initial clinical assessment, and b) after performing lung ultrasound (LUS) for LUS arm or after chest radiography (CXR) and natriuretic peptide (NT-pro BNP) results for CXR arm. All patients will undergo CXR, those enrolled in the LUS arm, after sonographic evaluation. After discharge, the cause of patient's dyspnea will be determined by independent review of the entire medical records performed by two emergency physicians. In case of disagreement, a third expert physician will review entire medical records, and adjudicate the case.

NCT ID: NCT02097602 Completed - Stroke Clinical Trials

Correlation Between Reticulated Platelets and Major Adverse Cardiac and Cerebrovascular Events After Noncardiac Surgery

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

This is an observational study designed to monitor the course of the fraction of reticulated platelets and the correlation thereof to major adverse cardiac and cerebrovascular events after noncardiac surgery.

NCT ID: NCT02084992 Completed - Clinical trials for Congestive Heart Failure

A Study of a Technology-enabled Disease Management Program to Reduce Hospitalizations for Heart Failure

SpanCHFIII
Start date: June 2014
Phase: N/A
Study type: Interventional

This study will randomize participants with a diagnosis of congestive heart failure and at least one risk factor for hospitalization to either a tablet computer and web based disease management program or a telephone based disease management program. Both interventions are home based with heart failure education and symptom monitoring provided by nurse managers. The nurse managers are in close communication with both the participants and the participants' physicians . The components of the disease management program have been developed at Tufts Medical Center and the New England Quality Care Alliance with studies showing improved clinical outcomes, including reduced hospitalizations. The goal of this study is to transition this successful home monitoring and disease management program to a tablet computer and web-based implementation to both improve clinical outcomes (reducing hospitalizations and improving self-perceived health status) and improve provider-patient satisfaction. We hypothesize that the tablet computer based disease management will decrease heart failure hospitalizations.

NCT ID: NCT02083744 Completed - Clinical trials for Congestive Heart Failure

Project Fluido: Fluid Watchers

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

The long-term goal of this research is to determine whether a psychoeducational intervention will support self-care behaviors in Hispanic patients with heart failure. The specific goal of this study is to determine whether a culturally-appropriate psychoeducational intervention in Hispanic patients with heart failure, compared to a control group, will improve heart failure knowledge and self-care behaviors. We hypothesize that patients who receive the intervention will have improved heart failure self-care behaviors and depression scores as measured by the Self-Care Heart Failure Index and Patient Health Questionnaire.

NCT ID: NCT02078739 Completed - COPD Clinical Trials

Tele-yoga Program in COPD and Heart Failure

Tele-yoga
Start date: June 2013
Phase: N/A
Study type: Interventional

The combined diagnosis of chronic obstructive pulmonary disease (COPD) and heart failure (HF) is common but often missed because of similarities in clinical presentation, risk factors, and patient characteristics. The concurrent presence of both diseases worsens the limitations in exercise capacity and quality of life that patients experience with either disease alone. This pilot study will test the feasibility of a yoga program conducted in patients' homes using multi-point interactive videoconferencing ("Tele- Yoga") for patients with combined COPD/HF diagnoses. The investigators hypothesize that patients who receive a yoga program at home, compared to an educational control group, will experience fewer physical symptoms and better quality of life.