drugset / Trial / NCT05230901

Effect of Antifibrotic Therapy on Regression of Myocardial Fibrosis After Transcatheter Aortic Valve Implantation (TAVI) in Aortic Stenosis Patients With High Fibrotic Burden

NCT05230901

Phase 3 Unknown 300 enrolled University Medical Center Goettingen
RandomizedParallel-groupOpen-labelTreatment

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.

Timeline

Start
2022-02-23
Primary completion
2025-06
Completion
2026-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Dihydralazine Small molecule 12.5 mg Oral
Subject Dihydralazine Small molecule 25 mg Oral
Subject Spironolactone Small molecule 25 mg Oral

Indications