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Heart Failure, Congestive clinical trials

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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: 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.

NCT ID: NCT00378950 Completed - Clinical trials for Heart Failure, Congestive

Educational Program for Various Health Literacy Levels to Improve the Health of Individuals With Heart Failure

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

Heart failure (HF) affects 5 million people in the United States. Health literacy, which is the ability to read and comprehend important medical information, plays an important role in the health of individuals with HF. This study will evaluate the effectiveness of an educational program developed for various levels of health literacy at improving medical outcomes and quality of life in individuals with HF.

NCT ID: NCT00377702 Completed - Clinical trials for Cardiovascular Diseases

Lifetime Risk for Cardiovascular Disease Among Non-White Ethnic Groups

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

Cardiovascular disease (CVD) is one of the leading causes of death in the United States. Currently, there is little information about the lifetime risk of CVD among non-white ethnic groups. This study will analyze data from participants in several ongoing clinical studies to identify the lifetime risk for CVD among various ethnicities.

NCT ID: NCT00376116 Completed - Clinical trials for Heart Failure, Congestive

Home Monitoring in Cardiac Resynchronisation Therapy

HomeCARE
Start date: March 2005
Phase: N/A
Study type: Observational

In spite of success in the management of heart failure, repetitive rehospitalisation and high mortality rate remain a serious problem. Recent studies, especially the COMPANION trial, have demonstrated that cardiac resynchronisation therapy (CRT) reduces mortality and rehospitalisation in heart failure patients. There is also evidence that telemonitoring of heart failure patients potentially reduces both mortality and morbidity. Recently, a Home Monitoring (HM) function has been integrated into BIOTRONIK CRT-defibrillators and CRT-pacemakers with a view of harnessing the powerful combination of CRT with close remote monitoring of heart failure patients. It is possible now to transmit predefined parameters on a daily basis from the implanted devices to a web-based platform accessible by patients' physicians. Our study evaluates clinical usefulness of Biotronik HM function in CRT-defibrillators and CRT-pacemakers.

NCT ID: NCT00366639 Completed - Clinical trials for Heart Failure, Congestive

Registry for Acute Decompensated Heart Failure Patients

Start date: October 2001
Phase: N/A
Study type: Observational

The purpose of the ADHERE study is to develop a multi-center, observational, open-label registry of the management strategies of patients treated in the hospital for acute Heart Failure in the United States.

NCT ID: NCT00364416 Completed - Clinical trials for Heart Failure, Congestive

Longitudinal Registry for Advanced Heart Failure Patients

Start date: October 2002
Phase: N/A
Study type: Observational

The purpose of this study is to gather information to better understand the characteristics, medical management techniques and outcomes of patients with chronic severe Heart Failure (HF).

NCT ID: NCT00364325 Completed - Clinical trials for Heart Failure, Congestive

Registry for Acute Decompensated Heart Failure Patients Admitted to the ER

Start date: July 2004
Phase: N/A
Study type: Observational

The purpose of this study is to collect data on the medical management of patients presenting to the Emergency Department who are treated for Acute Decompensated Heart Failure (ADHF) in a hospital setting that has incorporated a disease management program for heart failure.