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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: NCT02205411 Terminated - Heart Failure Clinical Trials

Clinical Trial to Evaluate the the ReliantHeart HeartAssist 5® VAD System in Patients Awaiting Heart Transplantation

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

The purpose of the study is to evaluate the safety and effectiveness of the ReliantHeart HeartAssist 5® VAD System in patients listed for heart transplantation and at risk of death from refractory end-stage heart failure.

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: NCT02152566 Terminated - Clinical trials for Congestive Heart Failure

Nasal High Flow Therapy for the Treatment of Respiratory Insufficiencies During Sleep

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

Respiratory insufficiencies during sleep can lead to reductions in the level of oxygen in the blood during the night, which has been shown to contribute to a range of morbidities. The purpose of this study is to assess the possibility that a nasal high flow therapy device may be able to treat respiratory insufficiencies, by stabilizing breathing and preventing reduction in blood oxygen. Heart failure patients will be screened at a heart failure clinic, and will be asked to undergo an overnight sleep study to determine is they exhibit respiratory insufficiencies during sleep. This sleep study may be completed in the sleep laboratory (attended polysomnography, PSG) or in-home (in-home polygraphy, PG). If they are diagnosed with respiratory insufficiencies, they will be asked to attend further overnight studies to see if treatment with nasal high flow therapy can be used to stabilize breathing.

NCT ID: NCT02147340 Not yet recruiting - Clinical trials for Congestive Heart Failure

External Sensors for remoTe MoniToring of Heart Failure Patients With Implantable Defibrillators

ESTIMATE-HF
Start date: June 2014
Phase: N/A
Study type: Observational

This study has been designed to describe the use of Remote Patient Management (RPM) systems equipped with sensors for the measurement of weight and blood pressure in an Italian health care setting, verifying their efficacy and efficiency for the remote management of heart failure patients with implantable defibrillators. Moreover, their ease of use and acceptance by physician and patient will be assessed.

NCT ID: NCT02139449 Recruiting - Clinical trials for Congestive Heart Failure

Prospective Study on Prognosis of Cardiac Resynchronized Therapy (CRT), Implantable Cardioverter Defibrillator (ICD) Implantation in Patients With Congestive Heart Failure (CHF)

Start date: April 2014
Phase:
Study type: Observational

CRT and ICD has known as decreasing cardiac mortality in patient with heart failure. Especially, it has reported that CRT improved cardiac systolic function, quality of life of patients with heart failure. However, CRT and primary ICD was not generalized in Korea. So the investigators will register patients who implant CRT or ICD (primary), and follow them up. During scheduled follow up, all patients will perform echocardiography, 6 minute walking test, EKG, Holter monitoring and questionnaire on QOL.

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: NCT02121158 Terminated - Clinical trials for Coronary Artery Disease

Efficacy and Safety of Implantable Cardioverter-Defibrillator (ICD) Implantation in the Elderly

I-70
Start date: August 7, 2015
Phase: N/A
Study type: Interventional

The overall aim of this trial is to study the safety and efficacy of ICD implantation as a primary prevention strategy of sudden cardiac death in patients 70 years and older. This study will assess the many competing factors involved with ICD implantation including 1) the impact on mortality, especially in the context of a declining rate of sudden death with advanced age, 2) the tolerability of the powerful therapeutic action of the device, and 3) the impact on quality of life.

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.