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Heart Failure, Congestive clinical trials

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NCT ID: NCT00414401 Completed - Clinical trials for Heart Failure, Congestive

Clinical Reminders in Test Reports to Improve Guideline Compliance

Start date: May 2001
Phase: N/A
Study type: Interventional

Although beta-blockers are known to prolong survival for patients with reduced left ventricular ejection fraction, their use in the community and the VA is suboptimal.

NCT ID: NCT00409916 Recruiting - Clinical trials for Heart Failure, Congestive

PREVENT-HF: Prevention of Heart Failure Events With Impedance Cardiography Testing

Start date: January 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether outpatient therapeutic management guided by impedance cardiography (ICG), in addition to standard clinical assessment, will result in a longer time in days to the first heart failure hospitalization than therapy guided by clinical assessment alone.

NCT ID: NCT00404872 Completed - Clinical trials for Cardiovascular Diseases

Evaluating the Relationship Between Fatty Acids and Heart Disease

Start date: January 1989
Phase: N/A
Study type: Observational

Cardiovascular disease (CVD) affects millions of people in the United States; each year, more people die from CVD than from any other disease. Individuals with low levels of n-3 fatty acids and high levels of trans-fatty acids may have an increased risk of developing CVD. This study will evaluate the link between fatty acids and the presence of CVD in older adults.

NCT ID: NCT00400985 Completed - Clinical trials for Heart Failure, Congestive

Sensitivity of the InSync Sentry OptiVol Feature for the Prediction of Heart Failure

SENSE-HF
Start date: January 2005
Phase: N/A
Study type: Interventional

The SENSE-HF study is a prospective, observational, international multi-center study prospectively evaluating the sensitivity and positive predictive value of the OptiVol Fluid Trends data in predicting Heart Failure related hospitalizations and health care utilizations associated with signs and/or symptoms of pulmonary congestion, and to define OptiVol clinical guidelines for subject therapy management.

NCT ID: NCT00399594 Completed - Clinical trials for Heart Failure, Congestive

Effect of Targeting Left Ventricular Lead Position on the Rate of Response to Cardiac Resynchronization Therapy.

INCREMENTAL
Start date: March 2011
Phase: Phase 2/Phase 3
Study type: Interventional

Identifying & optimizing strategies to reduce the burden of heart failure is vital. Despite advances in pharmacotherapy, patients with heart failure are at high risk for death & hospitalization. Cardiac resynchronization therapy (CRT) synchronizes ventricular mechanical activity, improves cardiac output & reduces HF symptoms. However, ~50% of patients do not clearly respond to CRT. Sub-optimal placement of the LV pacing lead appears to be an important reason for non-response. This study will assess whether targeted LV lead placement will result in an increased probability of CRT response at 52 weeks vs. usual (lateral wall) lead placement.

NCT ID: NCT00389649 Completed - Clinical trials for Heart Failure, Congestive

Effect of Chronic Changes in Heart Rate on Congestive Heart Failure

Start date: November 2001
Phase: N/A
Study type: Interventional

This will be a double blind randomized crossover study of patients with congestive heart failure and a heart rate dependent upon a permanent pacemaker. Thus, at all times the heart rate can be maintained at a set rate by adjusting the settings of the pacemaker. Acute and chronic effects of heart rates of 60, 75, and 90 beats per minute will be evaluated. The effect of heart rate will be determined by measuring ejection fraction by nuclear ventriculography, six minute walk distance, and peak oxygen consumption on a maximal exercise test.

NCT ID: NCT00387803 Completed - Clinical trials for Heart Failure, Congestive

Safety and Effectiveness of Cardiac Resynchronization Therapy With Defibrillation

Start date: February 1998
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study was to determine if cardiac resynchronization therapy when combined with defibrillation is safe and effective in the treatment of symptomatic heart failure.

NCT ID: NCT00385749 Recruiting - Clinical trials for Heart Failure, Congestive

Right Ventricular Defibrillation Lead Select Site Study

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

This study will compare single coil right ventricular defibrillation leads for implanted cardioverter/defibrillators (ICDs) in the apical and high septal locations. It is hypothesized that RV septal positions are at least as good as apical positions using formally measured defibrillation thresholds(DFTs), and that they may have long term advantages in reducing left ventricular dysfunction.

NCT ID: NCT00383630 Terminated - Clinical trials for Heart Failure, Congestive

Bone Marrow Cell Transplantation to Improve Heart Function in Individuals With End-Stage Heart Failure

Start date: September 2007
Phase: Phase 2
Study type: Interventional

Heart failure is a condition in which the heart is unable to pump enough blood to the body's other organs. A heart transplant may be necessary for some individuals with end-stage heart failure. Left ventricular assist devices (LVADs) can assist the heart in pumping blood, and are commonly used until a donor heart becomes available. Bone marrow cells injected into the heart may improve heart function and may lead to earlier LVAD removal. The purpose of this study is to evaluate the safety and effectiveness of injected bone marrow cells in improving heart function in individuals with LVADs who are awaiting heart transplants.

NCT ID: NCT00381030 Completed - Clinical trials for Heart Failure, Congestive

Effects of Carvedilol on Health Outcomes in Heart Failure

Start date: October 2002
Phase: Phase 4
Study type: Interventional

The purpose of our study was to determine if a strategy of starting a heart medication (Beta-blocker) before patients leave the hospital and then being seen by a nurse manager would reduce subsequent hospitalizations compared to usual care. Hypothesis: A nurse-directed heart failure management program with inpatient initiation of beta blockers will improve health outcomes in a vulnerable, predominantly Hispanic and African American population.