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Heart Failure clinical trials

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NCT ID: NCT01064037 Terminated - Heart Failure Clinical Trials

A Phase IIb Study to Investigate the Efficacy and Tolerability of Cinaciguat (150 µg/h, 100 µg/h, 50 µg/h) Given Intravenously to Subjects With Acute Decompensated Chronic Congestive Heart Failure (ADHF)

COMPOSE EARLY
Start date: April 2010
Phase: Phase 2
Study type: Interventional

A placebo controlled, double-blind and randomized study to assess different doses of a new drug (BAY58-2667) given intravenously, to evaluate if it is safe and can help to improve the well-being of patients with acute decompensated heart failure.

NCT ID: NCT01061580 Terminated - Clinical trials for Congestive Heart Failure

BMAC Enhanced Coronary Artery Bypass Grafting (CABG)

Start date: May 2010
Phase: Phase 1/Phase 2
Study type: Interventional

Injection of concentrated bone marrow cells into the myocardium during CABG procedure.

NCT ID: NCT01060293 Terminated - Clinical trials for Acute Decompensated Heart Failure

Dopamine in Acute Decompensated Heart Failure II

DAD-HF II
Start date: July 2009
Phase: Phase 4
Study type: Interventional

The aim of this study is to compare the effects of 1) high-dose furosemide, 2) low-dose furosemide, and 3) low-dose furosemide combined with low-dose dopamine on diuresis, clinical status, renal function, electrolyte balance, length of stay, and 60-day post-discharge outcomes in patients hospitalized with acute decompensated heart failure.

NCT ID: NCT01023438 Terminated - Clinical trials for Chronic Heart Failure

Strategies to Improve Prescribing in Heart Failure Patients

Start date: January 2010
Phase: N/A
Study type: Interventional

The purpose of the study is to assess whether primary care physicians may uptitrate recommended drug therapies in stable heart failure patients if educational material and specialist support including phone or mail consultation are provided

NCT ID: NCT01014884 Terminated - Heart Failure Clinical Trials

Coventry Outcomes Study of Seniors (COSS): A Comparative Effectiveness Study to Evaluate the Effect of a Multidisciplinary Team's Intervention on the Incidence of Nonelective Hospitalizations in a Medicare Population

COSS
Start date: November 2009
Phase: N/A
Study type: Interventional

The investigators are studying the impact of the interventions of a multidisciplinary team (MDT) - consisting of a Coventry case manager, social worker, and medical director, alongside a Medco specialist pharmacist - on the hospitalization rates of high risk seniors with chronic conditions, compared with a usual care approach. The study will also examine the impact on quality of life, medication adherence, medical costs, hospital readmission rates, and a variety of other important measures. The outcome of COSS may support a means to further enhance and develop a comprehensive care model program by leveraging the partnership between a health plan and a pharmacy benefit manager.

NCT ID: NCT01014611 Terminated - Heart Failure Clinical Trials

Impact of Heart Failure on Calcium Homeostasis and Mitochondrial Function in Human Skeletal Muscle

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

The aim of this project is to investigate the impact of heart failure (HF) on calcium homeostasis, mitochondrial function and oxidative stress in human skeletal muscle, before and after exercise training. The role playing by circulating factors such as cytokines and catecholamines will also be evaluated. 24 HF patients will be enrolled in the study: 12 class II NYHA HF volunteers with a fraction of ejection between 40% and 30 %, and 12 class III NYHA HF volunteers with a fraction of ejection lower than 30 %. They will be compared to 24 sedentary healthy volunteers, matched on age and physical activity.

NCT ID: NCT01011647 Terminated - Clinical trials for Acute Myocardial Infarction

Prevalence of Sleep Disordered Breathing

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

A novel technique in identifying unspecified sleep apnea has been developed. This technique uses signals typical acquired from a bedside monitor that is found in critical care environments. Those signals are then processed by a sleep analysis algorithm to provide an Apnoea Hypopnea Index (AHI) score. This study is intended to determine whether the prevalence of sleep disordered breathing identification among patients in a Coronary Care Unit (CCU) using this novel approach is significantly different than using routine techniques.

NCT ID: NCT01001312 Terminated - Heart Failure Clinical Trials

Safety and Efficacy of Direct Blood Volume Measurement in the Treatment of Heart Failure

TEAM-HF
Start date: October 2010
Phase: Phase 4
Study type: Interventional

Heart failure is a common cardiac condition affecting nearly 6 million Americans. Silent blood volume overload is common in patients with heart failure and is associated with increased risk of death. This study is designed to determine if adjustment of therapy based on direct measurement of blood volume will reduce risk of hospitalization and death when compared with therapy based on clinical assessment of blood volume in patients with chronic heart failure.

NCT ID: NCT00982852 Terminated - Clinical trials for Coronary Artery Disease

Intravascular Ultrasound Derived Virtual Histology and Intracoronary Serum Markers of Inflammation

Start date: December 2008
Phase: N/A
Study type: Observational

Patients enrolled will need treated with an IVUS- VH (intravascular ultrasound-derived virtual histology) which is an arterial stent procedure, that involves threading a tiny wire into the artery, followed by a balloon, a stent, or other device to treat a blocked artery, and often (though not always), a special ultrasound catheter to take pictures of the inside of the artery. Participants in the study, will have an additional procedure performed: a tiny tube will be advanced into the heart artery to collect a blood sample for research purposes, and a blood sample will be collected from the femoral (thigh) artery through the tube that will be placed there as a standard part of having this procedure. The blood that is collected will be analyzed for markers of inflammation or irritation in the blood (c-reactive protein, myeloperoxidase, Monocyte chemotactic protein-1), as well and a gene called Matrix Metallopeptidase 3, which is believe to influence the progression of plaque on the walls of arteries and the progression of coronary artery disease. .

NCT ID: NCT00968383 Terminated - Heart Failure Clinical Trials

Cardiovascular Magnetic Resonance for the Occluded Infarct-Related Artery Treatment

COAT
Start date: September 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether opening an occluded infarcted artery 3-28 days after an acute myocardial infarction in high-risk asymptomatic patients with preserved infarct zone viability improves left ventricular systolic function and volumes at 6 months follow-up. The secondary purpose is to assess the changes in myocardial tissue characteristics after late percutaneous coronary intervention (PCI).