Heart Failure With Preserved Ejection Fraction Clinical Trial
Official title:
Evaluation of GeranylGeranylAcetone in Heart Failure With Preserved Ejection Fraction
The goal of this double-blind randomized, placebo-controlled cross-over trial is to evaluate the effectiveness of GerenylGeranylAcetone (GGA) in patients with Heart Failure with a preserved ejection fraction. The main questions it aims to answer are: - What is the effect of GGA on diastolic function? - What is the effect of GGA on endothelial function? Main study tasks: - Participants will be treated with either GGA or placebo for 13 weeks. After this they will have a break (wash-out) period for 6 weeks and then cross over to the other study arm. - Cardiac function will be measured using echocardiogram in all participants - Renal measurements and endothelial measurements will be performed on the participants. - Participants will perform a 5 minute walking distance test for functional capacity. - Participants will fill out questionnaires to score signs & symptoms. Researchers will compare the patients to themselves to see if the drug improves diastolic- and endothelial function.
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