Clinical Trials Logo

Clinical Trial Summary

The aim of the study is to evaluate the effect of antifibrotic therapy on regression of myocardial fibrosis after TAVI in patients with baseline high fibrotic burden. Therefore, patients will be treated with Spironolactone in addition to standard of care, Spioronolactone + Dihydralazine in addition to standard of care or according to standard of care alone without any study medication. First, differences between patients in the control arm and patients randomized to anti-fibrotic therapy will be analyzed. The second analysis will determine, whether dihydralazine medication in addition to spironolactone is able to increase a potential antifibrotic effect. Myocardial fibrosis will be assessed by cardiac magnetic resonance imaging (CMR) before TAVI and 1 year after. Quantification of potentially irreversible replacement fibrosis will be carried out by late gadolinium enhancement (LGE), and quantification of the potentially reversible diffuse interstitial fibrosis will be performed by measurement of the extracellular volume fraction (ECV), thereby deriving matrix volume and cell volume.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05230901
Study type Interventional
Source University Medical Center Goettingen
Contact Miriam Puls, Prof.
Phone +49 551 3910958
Email dr.m.puls@med.uni-goettingen.de
Status Recruiting
Phase Phase 3
Start date February 23, 2022
Completion date March 2026