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Recruiting NCT05750173

The EASE-IT CT Registry

Trial Parameters

Condition Transcatheter Aortic Valve Implantation (TAVI)
Sponsor Institut für Pharmakologie und Präventive Medizin
Study Type OBSERVATIONAL
Phase N/A
Enrollment 150
Sex ALL
Min Age 75 Years
Max Age N/A
Start Date 2023-09-01
Completion 2025-08
Interventions
Streamlining of the pre-procedural patient pathway

Brief Summary

ICA is not always required for a pre-TAVI workup of octogenarians and can be substituted by CTA resulting in a streamlined pre-procedural workup of patients without compromising patient safety.

Eligibility Criteria

Inclusion Criteria: Investigational CTA-only Cohort * Consecutive adult patients ≥ 75 years * Consecutive patients with severe AS (symptomatic or asymptomatic) with a guideline-based indication to undergo implantation of a transcatheter heart valve of the SAPIEN family * Ability to undergo CTA * Patient is scheduled to undergo a 30 Day and 3 Months follow-up CTA+ICA control Cohort * Consecutive adult patients ≥ 75 years * Consecutive patients underwent implantation of a transcatheter heart valve of the SAPIEN family because of severe aortic stenosis * Ability to undergo CTA and ICA Exclusion Criteria: investigational CTA-only Cohort * Patients with already diagnosed proximal stenosis of the left anterior descending artery (LAD) OR the left main coronary artery (LM) ≥50% * Any prior coronary revascularization / prior aortic valve replacement * Life expectancy below 12 months * Lack of informed consent / data protection statement CTA+ICA control Cohort * Patients diagnosed with proximal

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