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Congestive Heart Failure clinical trials

View clinical trials related to Congestive Heart Failure.

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NCT ID: NCT01817803 Withdrawn - Clinical trials for Congestive Heart Failure

A Prospective, Single-center, Open-label, Pilot Study to Compare the Effectiveness and Safety of Diuretics Add-On Strategy in Chronic Heart Failure Patients (DIOS 1)

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

To compare the effectiveness and safety of diuretics add-on strategy in chronic heart failure patients

NCT ID: NCT01787851 Withdrawn - Clinical trials for Congestive Heart Failure

Study of the Acute Effects of Triheptanoin in Heart Failure

ACETO-TCA
Start date: February 2013
Phase: Phase 1/Phase 2
Study type: Interventional

Patients with dilated cardiomyopathy who present for indwelling right heart catheterization will be enrolled and randomized to either control or triheptanoin oil for five days. Hemodynamics will be assess serially.

NCT ID: NCT01375361 Withdrawn - Clinical trials for Congestive Heart Failure

Nebulized Albuterol for Congestive Heart Failure Exacerbation

ACHE
Start date: April 2009
Phase: Phase 2/Phase 3
Study type: Interventional

This is a randomized trial of the use of Albuterol in the setting of acute decompensated Congestive Heart Failure with radiographic evidence of Cardiogenic Pulmonary Edema.

NCT ID: NCT01337349 Withdrawn - Clinical trials for Congestive Heart Failure

Effects of Pentoxiphylline on Left Ventricular (LV) Systolic Function Indices and Circulating Biomarkers in Patients With Chronic Congestive Heart Failure (CHF)

PENT-CHF
Start date: July 2010
Phase: N/A
Study type: Interventional

This is a prospective, double blinded randomized clinical study to evaluate the Effects of Pentoxifylline on left ventricular systolic function indices and circulating biomarkers in patients with chronic congestive heart failure. A few studies all focused in Africa have consistently shown marked beneficial effects of pentoxifylline in improvement of left ventricular size and systolic function along with marked decrease in biomarkers of heart failure and apoptosis markers on top of standard CHF therapy. Furthermore pentoxifylline was shown to have negligible effects on heart rate, blood pressure in those studies. Limitations of these studies are that they are largely single center originating in the African subcontinent and have never been tested in the North American population, particularly Caucasians. Despite major advances in medical therapy for congestive heart failure, it is still one of the leading causes of morbidity and mortality in North America. Most medications tested for improvement of Ejection Fraction with the exception of Beta-Blockers and Ace-Inhibitors have been associated with worsening mortality. Pentoxifylline is a medication that has negligible effects on myocardial oxygen consumption, yet promising effects on inflammatory markers seen in CHF with the possibility of improvement in LV systolic function and symptomology and may prove to be a useful addition for CHF patients. This would prove to be especially useful, particularly when associated with no major side effects.

NCT ID: NCT01082601 Withdrawn - Atrial Fibrillation Clinical Trials

Catheter Ablation for Atrial Fibrillation and Heart Failure

Start date: April 2010
Phase: N/A
Study type: Observational

To compare heart function, symptoms, exercise capacity and quality of life in patients with Congestive Heart Failure (CHF) and Atrial Fibrillation (AF)before and after catheter ablation. Hypothesis: Restoration and maintenance of sinus rhythm by catheter ablation, without the use of antiarrhythmic drugs, in AF and CHF improves heart failure status.

NCT ID: NCT00789100 Withdrawn - Clinical trials for Chronic Obstructive Pulmonary Disease

Evaluation of Remote Patient Monitoring.

Start date: February 2009
Phase: N/A
Study type: Observational

Nottingham Primary Care Trust has launched telemonitoring to support: independent living and self-management ability of people with congestive heart failure (CHF), chronic obstructive pulmonary disease (COPD) and co-morbidities; and reduce the health care utilisation associated with these patients, including the number of hospitalisations, GP visits and community matron and specialist community nurse home visits. The Multidisciplinary Assessment of Technology Centre for Healthcare (MATCH) will evaluate the technology and its impact of this telemonitoring system on quality of care (i.e. process measures), patient outcomes and direct healthcare costs from an NHS perspective.

NCT ID: NCT00699361 Withdrawn - Clinical trials for Congestive Heart Failure

Influence of Pantoprazole on Human Myocardial Contractility at Patients With Congestive Heart Failure

Start date: August 2008
Phase: Phase 3
Study type: Interventional

Recently literature revealed facts, that show H+/K+ ATPase expression is not limited tot he stomach. H+/K+ ATPase was also found in smooth muscle cells and in other tissues (McCabe, R.D. et al., Am J Physiol. 1992). For myocard a localisation is only proven for rats yet (Beisvag, V. et al., Acta Physiol Scand. 2003). Moreover biochemical hints lead us to a highly probability of a myocardial H+/K+ ATPase (Nagashima, R. et al., Jpn Heart J. 1999).

NCT ID: NCT00583921 Withdrawn - Atrial Fibrillation Clinical Trials

Ventricular Rate Regularization for Improved Quality of Life in Patients With CHF and AF

VRR
Start date: n/a
Phase: N/A
Study type: Observational

Single center investigator initiated sponsored by Guidant Boston Scientific Corp. to evaluate the benefit of ventricular rate regularization (VRR) in patients with congestive heart failure (CHF) and significant atrial fibrillation (AF) burden.

NCT ID: NCT00483236 Withdrawn - Clinical trials for Congestive Heart Failure

Prospective Study Looking at Quality of Life Measures in Non-ischaemic Cardiomyopathy After Mitral Valve Repair

Start date: December 1, 2007
Phase:
Study type: Observational

- Chronic severe mitral regurgitation can lead to symptoms and left ventricular dysfunction. - The purpose of this study is to prospectively follow patients with non-ischaemic cardiomyopathy who are eligible for mitral valve repair surgery and primarily measure the quality of life through the Minnesota Living with Heart Failure Questionnaire & the Kansas City Cardiomyopathy Questionnaire.

NCT ID: NCT00428103 Withdrawn - Clinical trials for Congestive Heart Failure

Effects of Mitral Valve Repair With the Geoform Ring on Cardiomyopathy

Start date: October 2006
Phase: N/A
Study type: Interventional

The primary aim of this study is to assess the changes on the shape and function of the left ventricle in patients with severe mitral valve regurgitation due to congestive heart failure and cardiomyopathy who undergo mitral valve reconstruction with a Geoform ring. Three-dimensional echocardiogram will be used for precise evaluation of the shape and function of the ventricle.