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Biomarkers of Inflammation and Fibrosis in Conduction Disorders After TAVI

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Trial details

Who runs it
Clinical Hospital Center Rijeka
Trial code
NCT07201363
Record updated
6 October 2025
Original description
Prediction of conduction disorders (CDs) in patients with severe aortic stenosis (AS) undergoing transcatheter aortic valve implantation (TAVI) is an important and complex process with a significant impact on patient outcomes. The goal of this observational prospective trial is to investigate the role of pre-procedural values of systemic biomarkers of inflammation and fibrosis in the prediction of new-onset CDs and permanent pacemaker implantation (PPI) in patients undergoing the TAVI procedure.Read full original descriptionShow less

The Role of Inflammation and Fibrosis in the Development of Conduction Disorders After Transcatheter Aortic Valve Implantation

Prediction of conduction disorders (CDs) in patients with severe aortic stenosis (AS) undergoing transcatheter aortic valve implantation (TAVI) is an important and complex process with a significant impact on patient outcomes. The goal of this observational prospective trial is to investigate the role of pre-procedural values of systemic biomarkers of inflammation and fibrosis in the prediction of new-onset CDs and permanent pacemaker implantation (PPI) in patients undergoing the TAVI procedure.

Inclusion: Written consent to participate in the trial; Diagnosis of severe AS according to current European Society of Cardiology (ESC) guidelines for valvular heart disease.

Exclusion: Corticosteroid or other immunosuppressive therapy; Permanent pacemaker implanted previously; An acute myocardial infarction within three months before the procedure; A surgical procedure within three months before the procedure; Previous surgical or transcatheter aortic valve replacement/implantation; Acute infectious disease; Chronic inflammatory or autoimmune disease; Active malignant disease; Liver disease accompanied by dysfunction; End-stage chronic kidney disease (eGFR <15 ml/min).

ClinicalTrials.gov NCT07201363