RecruitingNot ApplicableNCT05788770

Preoperative CT-imaging with Patient-specific Computer Simulation in Transcatheter Aortic Valve Replacement

Preoperative CT-imaging with Patient-specific Computer Simulation in Transcatheter Aortic Valve Replacement: a Randomized Controlled Trial


Sponsor

Romy Hegeman

Enrollment

454 participants

Start Date

Apr 6, 2022

Study Type

INTERVENTIONAL

Conditions

Summary

Combining routine preoperative CT imaging with patient-specific computer modelling predicts the interaction between different sizes of transcatheter aortic valve replacement devices at different implantation depths and the patient's unique anatomy (including post-implantation deformation) allowing preoperative evaluation of the risk for paravalvular leakage and conduction disorders. The objective of this randomized controlled trial is to evaluate whether pre-operative CT-imaging with advanced computer modelling and simulation (FEops HEARTguide™) adequately predicts procedural outcomes in TAVR procedures, whether it leads to changes of preoperative decisions and whether or not this leads to improved outcome in TAVR procedures.


Eligibility

Min Age: 18 Years

Inclusion Criteria4

  • Primary symptomatic severe aortic valve stenosis
  • Accepted for TAVR, either by transfemoral, transsubclavian or transapical access
  • Plan to implant one of the following transcatheter heart valves for which FEops HEARTguide™ is available (CoreValve™ Evolut™ R, and Evolut™ PRO and Evolut™ PRO+ (Medtronic, Minnesota, USA), ACURATE neo™ and ACURATE neo 2™ (Boston Scientific, Marlborough, MA, USA)
  • Informed consent

Exclusion Criteria6

  • Previous surgical aortic valve replacement
  • Permanent pacemaker at baseline
  • Emergency procedure
  • Poor CT image quality (disabling computer-simulation, i.e. generation of 3D anatomical models will not be possible with poor CT image quality), for example because of motion artifacts due to the presence of other implanted devices affecting the region of interest
  • Patient who did not agree to the informed consent and/or refused to participate
  • Patient unable to understand the informed consent/study

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

OTHERFEops HEARTGuide

FEops HEARTGuide added to routine preoperative CT imaging. Results of the computer modelling will be discussed with TAVR implanting team prior to and during the procedure.


Locations(2)

Vienna General Hospital

Vienna, Austria

St. Antonius Hospital

Nieuwegein, Utrecht, Netherlands

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT05788770


Related Trials