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Chronic Heart Failure clinical trials

View clinical trials related to Chronic Heart Failure.

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NCT ID: NCT02732990 Recruiting - Clinical trials for Chronic Heart Failure

Peripheral Metabolic Function in Chronic Heart Failure Patients

Start date: February 2014
Phase: N/A
Study type: Interventional

Exercise intolerance is a major limiting symptom in patients with CHF. However the poor correlation between the hemodynamic parameters of left ventricular performance at rest and exercise performance has led to the concept that peripheral factors such as muscle perfusion and muscle metabolism play a role as determinants of exercise capacity.

NCT ID: NCT02563873 Recruiting - Clinical trials for Chronic Heart Failure

Bowditch Revisited: Defining the Optimum Heart Rate Range in Chronic Heart Failure

Start date: October 2015
Phase: N/A
Study type: Interventional

The investigators are examining the relationship between heart rate and heart contraction in patients with heart failure and pacemakers, aiming to improve quality of life.

NCT ID: NCT02559128 Recruiting - Insulin Resistance Clinical Trials

The Role of Insulin Resistance in Patients With Heart Failure and Type 2 Diabetes

CARMET2
Start date: December 2013
Phase:
Study type: Observational

The purpose of this cross-sectional comparative 2x2 trial study is to compare the degree of insulin resistance, myocardial function and selected metabolic parameters and to explore the pathophysiological mechanisms by which insulin resistance is implicated in development of chronic heart failure (HF) in patients with type 2 diabetes and prediabetes (T2D). Investigators hypothesize that patients with heart failure will be insulin-resistant and will display metabolic abnormalities as patients with diabetes.

NCT ID: NCT02493907 Recruiting - Clinical trials for Chronic Heart Failure

Corrected Left Ventricular Electrical Delay Predicting Response to Cardiac Resynchronization Therapy

Start date: December 2014
Phase: N/A
Study type: Observational

Cardiac resynchronization therapy (CRT) is a well-established treatment for patients with severe systolic heart failure (HF) and ventricular desynchronization. Despite the consistently observed structural and functional improvements as well as reductions in HF events and mortality in large multicenter randomized trials, 30% patients remain classified as nonresponders. Present evidences showed that QRS duration was the most effective parameter to predict responsivity of CRT in patients with severe HF. But some studies showed that QRS duration could be influenced by obesity and gender. Accordingly, the simple QRS interval width of body surface electrocardiograph should not be the most satisfactory parameter for screening patients suitable for CRT. Recent study showed that left ventricular electrical delay, as measured by the time from the onset of QRS to the LV electrogram peak (QLV), predicted CRT response. At long QLV intervals, atrioventricular optimization (AVO) can increase the likelihood of structural response to CRT. However, it is unclear whether it is suitable for Chinese patients. The investigators would like to validate this relation in a Chinese population and explore if a corrected QLV might do better to predict the responsivity of CRT.

NCT ID: NCT02486887 Recruiting - Clinical trials for Chronic Heart Failure

Home Electronic Monitoring of Chronic Heart Failure

MEDIC
Start date: June 2015
Phase: N/A
Study type: Interventional

The main objective of the study is to evaluate the effect of telemonitoring on mortality and rehospitalization due to heart failure on patients with chronic heart failure which have follow an educational program compared to a conventional follow-up during 1 year. The secondary objectives of the study are : - Evaluate the cost of health - Qualitatively evaluate telemonitoring on uses - Evaluate quality of life

NCT ID: NCT02335801 Recruiting - Clinical trials for Chronic Heart Failure

The TOSCA Registry: Hormonal and Metabolic Deficiencies in Chronic Heart Failure

TOSCA
Start date: April 2013
Phase:
Study type: Observational [Patient Registry]

The objective of this study is to determine whether the presence of metabolic alteration and anabolic deficiencies in patients with chronic heart failure are able to identify a subset of patients with poor outcome.

NCT ID: NCT02322034 Recruiting - Clinical trials for Chronic Heart Failure

Interval Training and Hormones in Chronic Heart Failure

Start date: January 2015
Phase: N/A
Study type: Interventional

The investigators aim at investigating whether 24-week high intensity interval training might exert beneficial effects by modulating neurohormonal axis in patients with chronic heart failure (CHF). Furthermore, the effect of detraining on neurohormonal axis in CHF patients will be evaluated.

NCT ID: NCT02292030 Recruiting - Clinical trials for Chronic Heart Failure

Cardioversion of Atrial Fibrillation Accompanied by Chronic Heart Faliure

Start date: November 2014
Phase: N/A
Study type: Observational

The purpose of this study is to explore the efficacy of low energy cardioversion on atrial fibrillation accompanied with chronic heart failure treated with HTEA or usual medicine.

NCT ID: NCT02282618 Recruiting - Clinical trials for Chronic Heart Failure

Effects of Cardiac Sympathetic Blockade in Patients With Chronic Heart Failure

Start date: May 2013
Phase: N/A
Study type: Observational

Although current pharmaceutical therapies have improved the survival rate in heart failure it remains a fatal disease and is associated with a poor 3-year survival. Increased sympathetic activity found in patients with heart failure plays an important role in the pathogenesis and development of the disease[Provide reference]. Excessive activation of sympathetic tone contributes to arrhythmogenesis, increased cardiac wall tension, and platelet aggregation, promoting a "vicious cycle[What cycle? Elaborate. ]" in these patients. High thoracic epidural anesthesia (HTEA) can reversibly and regionally block the cardiac sympathetic nervous system. The method was pioneered by Prof. Liu Fengqi in 1995, and he has accumulated clinical experiences from thousands of cases. His anecdotal experience indicates that the method can favorably improve intractable angina, dilated cardiomyopathy, and advanced heart failure. Though the method has been used to treat patients at our center for many years, there has been no prospective trial of its effects on cardiovascular function, or its efficacy to improve clinical outcomes. The investigators propose to investigate the immediate physiologic effect and clinical effectiveness of HTEA in treating heart failure.

NCT ID: NCT02137733 Recruiting - Clinical trials for Chronic Heart Failure

The Cardiac Insufficiency BIsoprolol Study in Japanese Patients With Chronic Heart Failure (CIBIS-J)

Start date: June 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the non-inferiority of bisoprolol to carvedilol by evaluating tolerability (The probability that administered maintenance dose reaches the maximum will be determined as an indicator) as a primary endpoint when bisoprolol or carvedilol is administered for 48 weeks to Japanese chronic heart failure patients. In addition, the safety and efficacy of bisoprolol will be investigated.