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Clinical Trial Summary

Transcatheter aortic valve implantation (TAVI) is a well known safe treatment for severe aortic stenosis. To perform TAVI safely, there is a need for two vascular entry (access) sites: the primary and secondary access sites. While the femoral approach remains the most common site for primary access, secondary access (which is needed for guidance during the procedure) has drawn little attention in trials of TAVI. The two secondary access sites most commonly used are the radial (through an artery in the wrist) and femoral (through an artery in the groin) access sites. Observational studies comparing the two have shown a lower risk of complications with radial access compared to femoral access, but there are no randomized controlled data to confirm these findings. Accordingly, investigators aim to undertake a multicenter, randomized controlled trial among patients who are undergoing transfemoral TAVI, to assess if radial access is superior to femoral access as a secondary access site.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06284837
Study type Interventional
Source The Alfred
Contact Jennifer Zhou, MBBS, BMedSc
Phone +61390763263
Email je.zhou@alfred.org.au
Status Recruiting
Phase N/A
Start date December 4, 2023
Completion date August 2025

See also
  Status Clinical Trial Phase
Recruiting NCT03984877 - Impact of Amyloidosis on TAVI Patients
Recruiting NCT04056832 - Left Ventricular Reverse Remodeling In Aortic Valve Replacement With Single Strip Pericardium Versus Mechanical Valve N/A