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Congestive Heart Failure clinical trials

View clinical trials related to Congestive Heart Failure.

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NCT ID: NCT01522378 Terminated - Clinical trials for Congestive Heart Failure

Cardiac Resynchronization and Iodine Meta-Iodobenzylguanidine (MIBG) Imaging

Start date: February 2012
Phase: Phase 1
Study type: Interventional

Subjects were recruited if their healthcare provider decided that they needed treatment with a special Internal Cardiac Defibrillator (ICD) called a biventricular ICD. The investigators did this study to see if part of the nerve organ, called the sympathetic nervous system, may be responsible for the improvement seen in patients that receive biventricular pacing. The investigators had three ways to measure sympathetic nervous activity: 1) by using a special blood sample, 2) by monitoring heart rhythm, and 3) by performing a special heart scan.

NCT ID: NCT01520714 Terminated - Clinical trials for Congestive Heart Failure

Effect of Posture on Left Ventricular (LV) Transvenous Lead Capture Thresholds (EXPECT)

EXPECT
Start date: December 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether changes in a patient's position affect LV capture thresholds in a clinically significant way.

NCT ID: NCT01516346 Completed - Heart Failure Clinical Trials

Vasodilator Therapy for Heart Failure and Preserved Ejection Fraction

Start date: January 2012
Phase: Phase 2
Study type: Interventional

The main objective is to test the effect of prolonged therapy (24 weeks) with isosorbide dinitrate ± hydralazine on arterial wave reflections (primary endpoint). Secondary endpoints include left ventricular (LV) mass, fibrosis and diastolic function) and exercise capacity (assessed via the 6-minute walk test) in patients with Heart Failure and Preserved Ejection Fraction (HFPEF). We will also test the hypothesis that the reduction in arterial wave reflections induced by vasoactive therapy will correlate with the improvement in exercise capacity, LV mass, fibrosis and diastolic function. Finally, we will assess whether the hemodynamic response to an acute dose of sublingual nitroglycerin (NTG) can predict the sustained changes in the reflected wave and other hemodynamic parameters in response to chronic vasodilator therapy.

NCT ID: NCT01513993 Completed - Clinical trials for Congestive Heart Failure

Remote Monitoring of Chronic Heart Failure in Veneto Region

Start date: October 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate whether telemonitoring of patients with chronic heart failure produces a reduction in the combined end point of all cause mortality and number of hospitalisations, and whether it improves health related quality of life. In addition, the trials evaluate the economic and organisational impact of the telemonitoring service and examine its acceptability by patients and health professionals.

NCT ID: NCT01503463 Completed - Clinical trials for Congestive Heart Failure

Remote Monitoring of Patients With CHF in Central Greece

RHCluster7GR
Start date: March 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate whether telemonitoring of patients with chronic heart failure produces a reduction in the combined end point of all cause mortality and number of hospitalisations, and whether it improves health related quality of life. In addition, the trials evaluate the economic and organisational impact of the telemonitoring service and examine its acceptability by patients and health professionals.

NCT ID: NCT01501331 Completed - Clinical trials for Congestive Heart Failure

Multiparametric Heart Failure Evaluation in Internal Cardioverter Defibrillators (ICD) Patients

MULTITUDE-HF
Start date: December 2011
Phase: N/A
Study type: Observational

The Boston Scientific Energen family is capable of measuring the respiratory rate trend (RRT) on a daily basis and transmission of data via the Remote Monitoring technology. This may result in early detection of imminent decompensation at a presymptomatic stage. The study will assess the respiratory trends correlation with clinically relevant heart failure events.

NCT ID: NCT01500759 Completed - Clinical trials for Congestive Heart Failure

Sleep-Disordered Breathing in Heart Failure - The SchlaHF-Registry

SchlaHF
Start date: November 2007
Phase:
Study type: Observational [Patient Registry]

Objective target of the registry is to investigate the prevalence of SDB as well as the clinical characteristics of patients with and without SDB as well as the predominant type of sdb. For this purpose data from patients suffering from chronic, symptomatic heart failure with impaired left ventricular ejection fraction will be collected prospectively.

NCT ID: NCT01481012 Terminated - Clinical trials for Congestive Heart Failure

The Epidemiology of Bleeding and Clotting in Patients Undergoing Heart Transplantation, Coronary Artery Bypass Graft Surgery,or Implantation of Left Ventricular Assist Devices

Start date: January 2006
Phase: N/A
Study type: Observational

The purpose of this study is to obtain data or information on how blood clotting factors are activated during open heart surgery. In particular, the investigators are interested in how blood clotting factors are activated by the heart-lung bypass machine and by left ventricular assist devices (LVAD). Patients on these two machines have an increased risk of bleeding and blood clot formation. This is because both machines stimulate the intrinsic coagulation pathway, one of the chemical pathways that cause blood to clot. The process of surgery itself also stimulates the "extrinsic coagulation pathway," the other chemical pathway that causes blood to clot. Stimulating these coagulation pathways can use up the body's clotting factors. As a result, patients may be at risk for both bleeding and blood clot formation. The investigators would like to study how the blood factors are activated during and after surgery, to help develop treatments to prevent bleeding and clot formation.

NCT ID: NCT01480921 Completed - Clinical trials for Congestive Heart Failure

Hospital Versus Home Based Exercise in Patients With Chronic Stable Heart Failure

PEAK-HF
Start date: July 2003
Phase: N/A
Study type: Interventional

The objective of this study is to compare the effect of monitored, home-based exercise versus hospital-based exercise on the quality of life of patients with congestive heart failure. Secondary objectives are to assess the effect of the intervention on exercise capacity and caregiver burden. The investigators hypothesize that the exercise training in the home-based environment will be superior to hospital based exercise training.

NCT ID: NCT01476995 Completed - Hypertension Clinical Trials

Prognostic Indicators as Provided by the EPIC ClearView

GBMC
Start date: September 2010
Phase: N/A
Study type: Observational

The objective of this study is to determine whether the finger tip images captured by the EPIC ClearView device, when analyzed via the ClearView software, produce a Response Scale that characterizes trends consistent with known diagnoses identified by medical doctors. Specifically, the investigators hypothesize that the organ system involving any of a series of known active diagnoses will be identified in the EPIC ClearView Response Scale report with the intention of providing potential triage capabilities.