MedPath

sPERMIdine supplemenTation on Metabolic, Neuronal and Cardiovascular Response to Exercise TRAINING

Not Applicable
Conditions
Heart Failure, Diastolic
Interventions
Dietary Supplement: spermidineLife
Dietary Supplement: Placebo
Registration Number
NCT05128331
Lead Sponsor
University Medicine Greifswald
Brief Summary

This study explores whether spermidine supplementation improves the metabolic, neurological-cognitive and cardiovascular response to structured exercise training in patients with heart failure with preserved ejection fraction. The investigators aim to show that a faster adaptation to exercise may improve long term adherence to a more active lifestyle.

Detailed Description

Heart failure with preserved ejection fraction is the largest unmet need in medicine. Exercise training is a pivotal lifestyle intervention which has been shown to have beneficial effects with regards to metabolic, neurological-cognitive and cardiovascular outcomes in these patients. Yet, not every patients responds equally fast to an exercise training intervention. This trial explores whether the supplementation of spermidine can increase the response to a structured aerobic exercise training. The investigators will recruit 30 patients who will either receive a spermidine supplement or a placebo. The study participants are invited for a first follow-up visit after four weeks. The exercise intervention starts at week 5 and continues for 12 weeks. Hence, overall there are three visits (baseline, week four and week twelve).

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
30
Inclusion Criteria
  • diastolic heart failure (E/e' > 8, left ventricular ejection fraction (LVEF) => 50 %, dyspnea)
Exclusion Criteria
  • nutritional supplements with polyamines
  • acute myo-, endo- or pericarditis
  • aortic valve stenosis (2nd degree)
  • cardiomyopathy or severe left ventricular hypertrophy (Interventricular septal end diastolic thickness or posterior wall thickness > 17 mm)
  • AV block (second degree)
  • pulmonary hypertension
  • thromboembolic event in the last six months
  • anemia
  • infection (with fever) within the last four weeks
  • cancer

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Spermidine supplementationspermidineLifeStudy participants are provided with spermidine supplementation
Placebo supplementationPlaceboStudy participants are provided with a placebo supplementation
Primary Outcome Measures
NameTimeMethod
Cardiorespiratory exercise capacity16 weeks

Change in cardiorespiratory exercise capacity (VO2peak) in ml/min/kg before and after of exercise training

Secondary Outcome Measures
NameTimeMethod
Diastolic function16 weeks

Change in diastolic function based on echocardiography (E/e')

Microvascular function16 weeks

Reactive hyperemia index assessed using EndoPat

Trial Locations

Locations (1)

Cardiovascular examination center of the University Medicine Greifswald

🇩🇪

Greifswald, Germany

© Copyright 2025. All Rights Reserved by MedPath