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Clinical Trial Summary

Microvascular function in patients undergoing Transcatheter Aortic Valve Implant (TAVI) for severe symptomatic aortic stenosis: association with myocardial fibrosis


Clinical Trial Description

Severe symptomatic aortic stenosis is commonly encountered in clinical practice, affecting close to 5% of individuals older than 65 years of age, and carries a dismal prognosis if left untreated.(1,2) Chronically increased left ventricular afterload triggers a compensatory myocardial response, ultimately leading to ventricular hypertrophy, aimed at reducing chronically increased wall tension an restore cardiac performance.(3) Hypertrophy ultimately results in maladaptive changes and ultimately leads to heart failure and eventually increased risk of cardiac mortality. Myocardial fibrosis and altered myocardial perfusion appear to play a role in progressive cardiac decompensation. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05326126
Study type Interventional
Source IRCCS San Raffaele
Contact Marco Ancona, MD
Phone +39/26437331
Email ancona.marco@hsr.it
Status Recruiting
Phase N/A
Start date July 8, 2021
Completion date October 30, 2025

See also
  Status Clinical Trial Phase
Not yet recruiting NCT02210351 - Evaluation of Association Between Apical Dysfunction and Trans Apical Access for TAVR, in Patients With Severe Aortic Stenosis, Undergoing Trans Apical Trans Catheter Aortic Valve Replacement (TAP-TAVR). N/A
Completed NCT02956915 - Evaluation of Length of Stay After TF-TAVI
Completed NCT04663334 - Change in Coronary Microcirculation and FFR After TAVI in Patients With Cardiovascular Comorbidities
Withdrawn NCT01742598 - Assessment of St Jude Medical Portico Re-sheathable Transapical Aortic Valve System N/A
Withdrawn NCT01927601 - Assessment of Neurologic Injury Subsequent to Transcatheter Aortic Valve Replacement: A Feasibility Study N/A
Completed NCT01787084 - Alternative Access Approaches for Transcatheter Aortic Valve Replace (TAVR) in Inoperable Patients With Aortic Stenosis N/A