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Heart Failure, Congestive clinical trials

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NCT ID: NCT00867984 Active, not recruiting - Clinical trials for Heart Failure, Congestive

Torsion Optimization to Reduce Symptoms and Improve Outcomes in Non-responders

TORSION
Start date: March 2009
Phase: Phase 3
Study type: Interventional

Approximately 40% of resynchronization therapy recipients do not appear to clearly benefit. These patients are termed 'non-responders'. This study will assess whether a heart ultrasound (echo) technique called 'torsion imaging' can be used to increase the likelihood of benefit from resynchronization therapy.

NCT ID: NCT00742508 Completed - Clinical trials for Chronic Heart Failure

A Phase I/II Clinical Study of SK&F-105517-D in Japanese Patients With Chronic Heart Failure

Start date: August 2008
Phase: Phase 1
Study type: Interventional

The primary objective of this study is to evaluate the safety and tolerability of SK&F-105517-D in japanese patients with chronic heart failure.

NCT ID: NCT00733590 Recruiting - Clinical trials for Heart Failure, Congestive

Prospective Observational Study of the ICD in Sudden Cardiac Death Prevention

PROSe-ICD
Start date: June 2003
Phase:
Study type: Observational

The overall hypothesis of this study is that subtle interactions between structural (substrate) and functional (trigger) abnormalities of the heart, some of which are genetically-determined, can be used to identify patients at high risk of sudden cardiac death (SCD). Such information may be used to better define patients most likely to benefit from replacement of an internal defibrillator (ICD). The prospective, observational study to enroll, categorize and follow patients who receive an ICD pulse generator replacement for primary prevention of SCD (PROSe-ICD) was established to : 1. to gain a better understanding of the biological mechanisms that predispose to SCD 2. to develop readily determined clinical, electrocardiographic, genetic and blood protein markers identify patients with an increased risk of dying suddenly

NCT ID: NCT00679549 Completed - Heart Failure Clinical Trials

The Role of Sleep Apnea in the Acute Exacerbation of Heart Failure

Start date: March 2008
Phase: N/A
Study type: Interventional

This study will evaluate whether treating sleep apnea while in the hospital would help heart failure, and assist recovery from the worsening of the heart function more than the current clinical standard of waiting for treatment until the subject have left the hospital. Heart failure affects more than 2% of the US population and is the only cardiovascular disorder with rising incidence. The annual cost of CHF in 2005 was $ 27.9 billion, large percentage of which is the cost of hospitalizations for exacerbation of CHF. Half of patients with CHF have some form of sleep apnea, and most of them go undiagnosed. Patients with CHF and OSA benefit from treatment with CPAP as an outpatient. The society can benefit from developing recommendations for approaching sleep apnea in the hospitalized CHF patient, which may shorten length of stay, improve functional status of discharged patient, and reduce rehospitalizations.

NCT ID: NCT00657280 Completed - Clinical trials for Heart Failure, Congestive

Study of the Effect of Sitagliptin on Glucose (Sugar) Metabolism in Patients With Heart Failure

S-001
Start date: April 2008
Phase: Phase 0
Study type: Interventional

This study will investigate the effects of sitagliptin, a medicine commonly used to treat type 2 diabetes, on the utilization of glucose by the heart in patients with heart failure which is not due to heart attacks. We hope to determine whether improving the heart's ability to use glucose in the blood may help improve the function of the heart as well. If so, this may suggest that even people who do not have frank diabetes but who do have heart failure may benefit from using this medication. This study will also investigate the effect of sitagliptin on the body's use of sugar, and of the effect of sitagliptin on blood flow to the heart.

NCT ID: NCT00645489 Completed - Clinical trials for Heart Failure, Congestive

A Family Intervention for Improving Self-Care of Patients With Heart Failure

Start date: March 2008
Phase: Phase 0
Study type: Interventional

This is a pilot study of a family-based educational program for patients with heart failure, and their family members.

NCT ID: NCT00559338 Completed - Clinical trials for Heart Failure, Congestive

Impact of Nesiritide Infusion for Decompensated Heart Failure in the Emergency Department

Start date: December 2003
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine if an 8hr infusion of nesiritide in the emergency department in the Acutely decompensated heart failure patients will decrease 30 day recidivism.

NCT ID: NCT00555360 Completed - Clinical trials for Heart Failure, Congestive

Enhancing Caregiver Support for Heart Failure Patients: the CarePartner Study

Start date: June 2009
Phase: N/A
Study type: Interventional

Informal caregivers, assisted by health information technology may help to fill the gaps in VA care management of heart failure patients by enhancing support for patients' treatment adherence, behavior changes, and symptom monitoring.

NCT ID: NCT00542503 Completed - Clinical trials for Heart Failure, Congestive

Using Magnetic Resonance Imaging to Predict People Who Are Likely to Develop Flash Pulmonary Edema (The PREDICT Study)

PREDICT
Start date: June 1, 2007
Phase:
Study type: Observational

Flash pulmonary edema is a sudden, abnormal build-up of fluid in the lungs. It is usually caused by heart failure and can be life threatening. The purpose of this study is to determine if a new form of magnetic resonance imaging (MRI) can identify abnormal blood flow to the lungs and predict increased risk of developing flash pulmonary edema among older adults.

NCT ID: NCT00541801 Completed - Clinical trials for Heart Failure, Congestive

Acoustic Cardiographic Assessment of Heart Function in Comparison to Doppler-echocardiography

Start date: March 2007
Phase: N/A
Study type: Interventional

In this study, the investigators sought to determine whether an acoustic cardiographic assessment of heart function is equivalent to Doppler-echocardiography in patients who are treated with cardio-toxic cytostatic agents.