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Clinical Trial Summary

The goal of this single-center, prospective, observational study is to validate a software package based on an artificial intelligence algorithm for automated non-invasive estimation of LVFP against invasively measured ones by left and right heart catheterization; In addition, the added value of this new automated software to detect increased LVEDP > 15 mm Hg compared to the current ASE/EACVI algorithm for assessing diastolic dysfunction and longitudinal left atrial strain during the reservoir phase will be evaluated.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05768698
Study type Observational [Patient Registry]
Source Istituto Auxologico Italiano
Contact Luigi Badano, MD, Ph.D.
Phone +390261911
Email l.badano@auxologico.it
Status Recruiting
Phase
Start date July 20, 2021
Completion date June 11, 2024

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