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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02732990
Other study ID # VEK-H-3-2013-048
Secondary ID
Status Recruiting
Phase N/A
First received November 6, 2014
Last updated April 4, 2016
Start date February 2014
Est. completion date August 2016

Study information

Verified date April 2016
Source Rigshospitalet, Denmark
Contact Gregers W Munch, MSc PhD
Phone +45 35459574
Email gregers.munch@regionh.dk
Is FDA regulated No
Health authority Denmark: Ethics CommitteeDenmark: Danish Dataprotection Agency
Study type Interventional

Clinical Trial Summary

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.


Description:

The pathophysiology behind the breathlessness and fatigue experienced by CHF patients during exercise remains unclear. Recent evidence suggests that the peripheral skeletal muscle, which becomes abnormal in heart failure, is the source of afferent signals which disrupt normal patterns of cardiorespiratory control. When CHF patients exercise, an inappropriately strong sympathetic response further limits exercise tolerance by evoking larger than normal increases in peripheral sympathetic activation at a faster rate than in healthy individuals. A consequence of this exacerbated sympathetic response may be the further sympathetic restraint of blood flow to the active skeletal muscles resulting in hypoperfusion of the muscle vascular bed and fatigue. Small muscle mass exercise training increases muscle oxidative capacity and improves aerobic work capacity in CHF patients. A range of studies is proposed here that will provide an integrative view of the mechanistic basis behind exercise intolerance in CHF and relate the intramuscular metabolic status to the autonomic control of hemodynamics during exercise. An understanding of the mechanistic basis of the improved exercise tolerance with training, independent of improved resting cardiac function, will yield important information regarding the integrated control of blood flow and metabolic demand in CHF and highlight the importance of maintaining the integrity of the peripheral musculature in CHF.


Recruitment information / eligibility

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

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Health Services Research


Related Conditions & MeSH terms


Intervention

Behavioral:
Exercise training
All gruoups will undergo 6 weeks of training intervention either with a small musclemass (one-legged exercise) or whole body exercise (two-legged cycling)

Locations

Country Name City State
Denmark Centre of Inflammation and Metabolism (CIM), Centre for Physical Activity Research Copenhagen

Sponsors (1)

Lead Sponsor Collaborator
Anders Rasmussen Rinnov

Country where clinical trial is conducted

Denmark, 

Outcome

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
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