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NCT ID: NCT00461019 Completed - Heart Failure Clinical Trials

CardioFitâ„¢ for the Treatment of Heart Failure

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

Congestive Heart Failure is the result of a number of diseases affecting the heart, causing the heart's failure to properly meet the body demands for blood circulation. In spite of advances in drug therapy, it remains a significant public health problem. Pharmacologic antagonism of the beta-adrenergic receptors shifting the autonomic balance in the direction of greater vagal influence is a well-proven treatment for heart failure patients, although there are patients who cannot tolerate, or only partially benefit from such a treatment. It has been proven in the past and well established that parasympathetic nerve stimulation can slow the rate of the heart and reduce the workload of the heart. Therefore, the potential benefit of vagus nerve stimulation, hence parasympathetic activation, for treatment of heart failure is substantial. In this study, the safety and efficacy of a new vagus nerve stimulating system will be evaluated. This study will compare whether the new device improves Heart Failure parameters in Class II - III Heart Failure patients.

NCT ID: NCT00460668 Completed - Lung Cancer Clinical Trials

The Effect of Post-thoracotomy Pulmonary Rehabilitation on Quality of Life

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

The purpose of this study is to evaluate the effects of an integrated multidisciplinary rehabilitation program on health related quality of life in the 12 months postoperative period in patients with an elective thoracotomy and to evaluate the effects of the program on general quality of life (SF-36), acute/chronic post-thoracotomy pain, impairment (changes in pulmonary function), disability (exercise capacity) and start to complete recovery (ECOG score of 0 or 1) 12 months postoperatively in patients with an elective thoracotomy.

NCT ID: NCT00460512 Completed - Schizophrenia Clinical Trials

An Efficacy, Safety And Tolerability Study of Flexibly Dosed Paliperidone Extended Release (ER) in Participants With Schizophrenia

PERFlexS
Start date: April 25, 2007
Phase: Phase 3
Study type: Interventional

The purpose of this study is to explore tolerability, safety and effectiveness of flexibly dosed paliperidone extended release (ER) in participants with schizophrenia (psychiatric disorder with symptoms of emotional instability, detachment from reality, often with delusions and hallucinations, and withdrawal into the self) previously unsuccessfully treated with an oral antipsychotic medication.

NCT ID: NCT00459771 Completed - Breast Cancer Clinical Trials

Evaluating the Effect of Candesartan vs Placebo in Prevention of Trastuzumab-associated Cardiotoxicity

Start date: June 2007
Phase: Phase 3
Study type: Interventional

Evaluating the effect of the angiotensin II-receptor (AT1) blocker candesartan vs placebo in prevention of trastuzumab-associated cardiotoxicity in patients with primary breast cancer treated with trastuzumab.

NCT ID: NCT00459706 Completed - Clinical trials for Rheumatoid Arthritis

Study Comparing Perceptions and Satisfaction for Two Different Delivery Mechanisms for Etanercept

Start date: September 2007
Phase: Phase 3
Study type: Interventional

The purpose of this study is to explore and compare the perceptions and satisfaction for two different delivery mechanisms for Etanercept (Etanercept Autoinjector and the Etanercept Prefilled Syringe) in patients with rheumatoid arthritis (RA).

NCT ID: NCT00459667 Completed - Clinical trials for Multiple Sclerosis, Relapsing-Remitting

BEYOND Follow-up: Betaferon®/Betaseron® Efficacy Yielding Outcomes of a New Dose

Beyond
Start date: May 2007
Phase: Phase 3
Study type: Interventional

The BEYOND Follow-Up study will give patients who participated in the preceding BEYOND study the opportunity to continue treatment with the 500µg dose of interferon beta (IFNB) 1b and will further investigate the safety and tolerability profile of interferon beta 1b 500µg during longer-term treatment.

NCT ID: NCT00457652 Completed - Clinical trials for Ischemia Reperfusion Injury

Does Caffeine Reduce Rosuvastatin-Induced Protection Against Ischemia-Reperfusion Injury?

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

Does caffeine reduce rosuvastatin induced protection against ischemia reperfusion injury?

NCT ID: NCT00457613 Completed - Shock Clinical Trials

Effects of Alkaline Phosphatase on Renal Function in Septic Patients

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

Septic shock is the most common cause of death in patients requiring intensive care. The kidney is one of the first organs to fail, stressing the importance to search for clinical interventions that may protect the kidneys during sepsis. Alkaline phosphatase functions as a host defence molecule and is present in many cells and organs (e.g. intestine, placenta, liver, kidney and bone). Alkaline phosphatase has a dual mode of action. First, it binds to and, subsequently, dephosphorylates lipopolysaccharide (LPS). Second, the enzymatic reaction product monophosphoryl-LPS is a non-toxic substance for mammals which acts as a partial antagonist on the LPS receptor complex. In several animal studies, administration of alkaline phosphatase attenuates the inflammatory response and reduces mortality. It is unknown whether these results can be extrapolated to septic patients . We studied the effects of alkaline phosphatse administration on kidney damage and function in patients with severe sepsis or septic shock.

NCT ID: NCT00457483 Completed - Clinical trials for Primary Hypertension

Nijmegen Antihypertensive Management Improvement Study

NAMIS
Start date: August 2007
Phase: Phase 4
Study type: Interventional

High blood pressure is an important risk factor for diseases of heart and blood vessels like myocardial infarction and stroke. Many patients are not treated to target blood pressures, even though good blood pressure lowering drugs are available. Not all blood pressure drugs are equally effective in individual patients. We hypothesize that individual patient characteristics can predict the best response on different blood pressure lowering drugs. In this study we will investigate whether a set of patient characteristics (anthropometric and laboratory) obtained before treatment may predict the blood pressure lowering response to representatives of two groups of drugs: those that inhibit renin-angiotensin system activity and those that decrease blood volume.

NCT ID: NCT00457405 Completed - Atherosclerosis Clinical Trials

Does a Seven Day Treatment With Dipyridamole Induce Protection Against Ischemia-Reperfusion Injury?

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

This study is performed to determine whether a seven day treatment with dipyridamole (slow release, 200mg twice daily) can induce a protective effect against ischemia-reperfusion injury, after ischemic exercise of the non-dominant forearm in healthy volunteers.