Chronic Heart Failure Clinical Trial
Official title:
Peripheral Metabolic Function in Chronic Heart Failure Patients: Key to Lessen the Cardiac Load
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.
Status | Recruiting |
Enrollment | 60 |
Est. completion date | August 2016 |
Est. primary completion date | August 2016 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | 40 Years to 70 Years |
Eligibility |
Inclusion Criteria: - New York Heart Association (NYHA) Class II - III - Ejection fraction <35% - Heart failure as a result of previous myocardial infarction - Optimal treatment (ACE-inhibitors, beta-blockers) - Stable heart failure - Patients with and without implantable cardioverter defibrillator (ICD) Exclusion Criteria: - Peripheral vascular disease with symptoms of atherosclerosis (intermittent claudication) - Aneurysm in a. femoral - Moderate to severe heart valve disease - Moderate to severe Chronic Obstructive Pulmonary Disease (COPD) with FEV1 <60% - Heart Failure Patients with Biventricular pacemaker (BVP) - Serious heart rhythm disturbances (arrhythmias such as atrial fibrillation and frequent premature ventricular contractions) - Myocardial infarction within the last month - Unstable angina (angina pectoris) - Renal failure (creatinine greater than 2.5 mg / dL) - Severe systemic disease of the nervous system, pulmonary or other severe organ involvement - BMI> 30 - Pregnancy |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Health Services Research
Country | Name | City | State |
---|---|---|---|
Denmark | Centre of Inflammation and Metabolism (CIM), Centre for Physical Activity Research | Copenhagen |
Lead Sponsor | Collaborator |
---|---|
Anders Rasmussen Rinnov |
Denmark,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change from baseline sympathetic nerve activity after 6 weeks of training | Sympathetic nerve activity, measured in plasma and dialysat with reference to nor-adrenaline. | 6 weeks | Yes |
Secondary | The effect of exercise training on exercise capacity in regards to oxygen uptake | Exercise capacity in regards to oxygen uptake (VO2peak) will be evaluated before and after the training intervention | 6 weeks | Yes |
Secondary | The effect of exercise training on exercise capacity in regards to maximal workload | Exercise capacity in regards to Workload during 2-legged cycling (Wattpeak) will be evaluated before and after the training intervention | 6 weeks | Yes |
Secondary | The effect of exercise training on exercise capacity in regards to a 6 min walk test | Exercise capacity in regards to a 6 min walk test (meters) will be evaluated before and after the training intervention | 6 weeks | Yes |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT03597646 -
The Effect of Kinesio Taping on Pulmonary Function and Functional Capacity in Patients With Chronic Heart Failure
|
N/A | |
Terminated |
NCT04065997 -
Apogee International
|
||
Withdrawn |
NCT03675113 -
Effect of Upper Extremity Aerobic Exercise Training on Exercise Capacity Patients With Chronic Heart Failure
|
N/A | |
Completed |
NCT02916160 -
Sacubitril-valsartan and Heart Failure Patients : the ENTRESTO-SAS Study
|
Phase 4 | |
Completed |
NCT03126656 -
Effects of Testosterone on Myocardial Repolarization
|
Phase 4 | |
Completed |
NCT02247245 -
The Influence of Heart Rate Limitation on Exercise Tolerance in Pacemaker Patients.
|
N/A | |
Completed |
NCT02268500 -
VAccination to Improve Clinical outComes in Heart Failure Trial: a Feasibility Study (VACC-HeFT)
|
Phase 4 | |
Completed |
NCT01919918 -
Muscle Afferent Feedback Effects in Patients With Heart Failure
|
Phase 1 | |
Terminated |
NCT01906957 -
Cognition and Exercise Training
|
N/A | |
Not yet recruiting |
NCT01669395 -
Severe Heart Failure and Homebased Rehabilitation - An Intersectoral Randomized Controlled Trial
|
N/A | |
Completed |
NCT00984529 -
Evaluation of Clinical Signs and Symptoms of Chronic Heart Failure in Patients Treated With Candesartan Cilexetil in Croatia
|
N/A | |
Recruiting |
NCT00863421 -
Sleep Disordered Breathing in Patients With Chronic Heart Failure
|
N/A | |
Completed |
NCT02840565 -
Tolerability, Pharmacokinetics and Pharmacodynamics of Six Multiple Rising Dose Regimens of BIA 5-453
|
Phase 1 | |
Completed |
NCT02441218 -
Effects of Ivabradine on Cardiovascular Events in Patients With Moderate to Severe Chronic Heart Failure and Left Ventricular Systolic Dysfunction. A Three-year International Multicentre Study
|
Phase 3 | |
Completed |
NCT00149409 -
Omega-3-Polyunsaturated Fatty-Acids (N3-Pufa) In Patients With Severe Chronic Heart Failure
|
Phase 2/Phase 3 | |
Terminated |
NCT05532046 -
A Study to Learn How Safe Study Drug BAY2413555 is, How it Affects the Body, and How it Moves Into, Through, and Out of the Body Over 4 Weeks of Use in Participants With Heart Failure and Implanted Cardiac Defibrillator or Cardiac Resynchronization Devices (ICD/CRT)
|
Phase 1 | |
Recruiting |
NCT04984928 -
Readmission Risk of Patients With Heart Failure.
|
||
Completed |
NCT02814097 -
A Study to Evaluate the Effects of 4 Weeks Treatment With Subcutaneous Elamipretide on Left Ventricular Function in Subjects With Stable Heart Failure With Preserved Ejection Fraction
|
Phase 2 | |
Active, not recruiting |
NCT05560737 -
ODYSSEE-vCHAT Mental Health Program for Heart Failure and Kidney Disease Patients
|
||
Recruiting |
NCT03286127 -
Palliative Outcome Evaluation Muenster I
|