Clinical Trials Logo

Heart Failure, Congestive clinical trials

View clinical trials related to Heart Failure, Congestive.

Filter by:

NCT ID: NCT00234104 Completed - Clinical trials for Heart Failure, Congestive

A Dose-finding Study of OPC-41061 in Treatment of Cardiac Edema (Congestive Heart Failure)

Start date: August 2004
Phase: Phase 2
Study type: Interventional

This drug is being developed to treat cardiac edema. The primary purpose of this study is to investigate the dose response for body weight in seven-day repeated oral administration of OPC-41061 at 15, 30, and 45 mg or placebo in patients with extracellular volume expansion secondary to CHF despite taking furosemide at 40 mg/d or more. This study is being conducted in Japan.

NCT ID: NCT00233480 Completed - Clinical trials for Heart Failure, Congestive

Statin Therapy in Heart Failure: Potential Mechanisms of Benefit

Start date: August 2005
Phase: Phase 4
Study type: Interventional

The goal of the investigators' study is to further understand the potentially beneficial effects of statin therapy in patients with heart failure. It is hypothesized that statins will 1) increase the heart's pumping ability 2) improve functioning of the sympathetic nervous system and 3) decrease immune activation in heart failure.

NCT ID: NCT00230932 Completed - Pain Clinical Trials

Help Veterans Experience Less Pain Study (HELP-Vets)

HELP-Vets
Start date: October 2005
Phase: N/A
Study type: Observational

Our purpose is to evaluate the reliability and validity of the '5th vital sign' in everyday practice settings and to compare the relationship of pain to other symptoms and pain treatment in patients with cancer, CHF, and patients with complex general medical illness and poor self-reported health.

NCT ID: NCT00213746 Completed - Clinical trials for Myocardial Infarction

Evaluation of Myocardial Viability by Means of Low-dose Dobutamine Gated SPECT (the DOGS Study)

Start date: October 2003
Phase: N/A
Study type: Observational

Viability assessment remains a clinical challenge in patient with coronary artery disease and left ventricular dysfunction. Several imaging modalities are available for evaluating myocardial viability, based either on perfusion or on contractile reserve analysis. Briefly, perfusion analysis is highly sensitive and contractile reserve highly specific. A combined analysis of both perfusion and contractile reserve has been proposed to improve the diagnostic accuracy in patient referred for a revascularization procedure. However, the value of this combined analysis has not been validated in unselected patients referred for viability assessment. The patients enrolled in the study will undergo a nitrate enhanced rest gated SPECT using a Tc-99m labeled tracer (sestamibi or tetrofosmine) followed by a second gated SPECT acquired during a low-dose dobutamine infusion (10 mcg/kg/mn). All patients will have a 6-month clinical and imaging follow-up, including physical examination and a nitrate enhanced rest gated SPECT using the same radiopharmaceutical. All treatments received during this 6-month period will be recorded, including medical therapy and coronary revascularization (angioplasty, stenting and CABG). Finally, the value of baseline perfusion and contractile reserve analysis in predicting left ventricular ejection fraction changes at 6-month follow-up will be evaluated.

NCT ID: NCT00204945 Completed - Clinical trials for Heart Failure, Congestive

Catheterization Laboratory Study: Acute Responses in Diastolic Heart Failure

Start date: February 2005
Phase: N/A
Study type: Interventional

1. Research question: What is the response of the heart's pumping function to changes in heart chamber pressures? 2. Experimental design: Patients undergoing routine cardiac catheterization will be studied. A thermodilution pulmonary artery catheter will be inserted through a venous sheath and threaded into the pulmonary artery. After several minutes of quiet rest, baseline hemodynamics will be obtained, including a determination of cardiac output using thermodilution techniques and 30 seconds of pressure recordings from the left ventricle and proximal aorta. In addition, a brief echocardiogram will be performed, to determine ejection fraction and indices of diastolic filling. Finally, arterial tonometry will be obtained in quick succession from the brachial, radial, femoral, and carotid arteries. Following the collection of baseline data, a bolus and infusion of nesiritide will be started. After 10 minutes of nesiritide infusion, with the drug still infusing, a full set of invasive hemodynamics will again be obtained, as well as brief echocardiographic and arterial tonometry examinations.

NCT ID: NCT00202579 Completed - Clinical trials for Heart Failure, Congestive

Efficacy and Safety of Ivabradine in Severe Congestive Heart Failure

Start date: September 2004
Phase: Phase 2
Study type: Interventional

To evaluate the effects on heart function of ivabradine administered to patients with severe chronic heart failure

NCT ID: NCT00195897 Terminated - Lymphoma Clinical Trials

Early Assessment of Anthracycline-induced Cardiotoxicity (CARDIOTOX)

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

Anthracycline-based chemotherapy is a key point of the treatment of patients with Hodgkin's and non-Hodgkin's lymphomas. However, cumulative doses are limited by cardiotoxicity, resulting in a marked left ventricular function impairment that may lead to heart failure. The standard clinical approach to monitoring for anthracycline cardiotoxicity is based on cardiac function monitoring using echocardiography or radionuclide angiography. The aim of this study is to evaluate the usefulness of biochemical markers of cardiac injury (troponin and NT-proBNP) and structural changes on cardiac MR in predicting anthracycline cardiotoxicity.

NCT ID: NCT00190359 Terminated - Clinical trials for Heart Failure, Congestive

Growth Hormone and Heart Failure

Start date: September 2000
Phase: N/A
Study type: Observational

Heart failure induces modification in several neurohormonal systems. The aim of this study is to determine if the growth hormone/IGF1 axis is modified in heart failure patients compared to healthy volunteers.

NCT ID: NCT00182065 Completed - Clinical trials for Heart Failure, Congestive

Heart Failure, Functional and Cognitive Decline, and Psychiatric Symptoms in Nursing Home Patients

Start date: March 1, 2004
Phase:
Study type: Observational

Heart failure is very common in the elderly, in whom it may lead to functional and intellectual problems. Functional problems include loss in the ability to perform basic tasks of daily living such as bathing or dressing. No studies have yet described the rate at which heart failure causes these problems to develop. This study aims to find out whether nursing home patients deteriorate more quickly with respect to function and intellect if they have heart failure. Participants will undergo a thorough health history and physical examination and will be followed every 3 months for up to a year. Over 30 nursing homes in Kitchener, Waterloo, Cambridge, and Hamilton, in South Central Ontario (Canada), are participating in this study. Every 3 months, participants will be reviewed with respect to function, intellect, mood and behaviours. Results between those with heart failure will be compared to those of people without heart failure. The results of this study will be used to plan further studies to see whether good treatment of heart failure can preserve function, intellect, and prevent depression and other mood problems.

NCT ID: NCT00181259 Recruiting - Clinical trials for Heart Failure, Congestive

Magnetic Resonance Spectroscopy Studies of Cardiac Muscle Metabolism

Start date: January 1988
Phase:
Study type: Observational

The metabolism of the heart provides the chemical energy needed to fuel ongoing normal heart contraction. Magnetic resonance spectroscopy is a technique used in a MRI scanner that can be used to measure and study heart metabolism directly but without blood sampling or obtaining tissue biopsies. One of the hypotheses this study aims to investigate is whether energy metabolism is reduced in heart failure and whether that contributes to the poor heart function.