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Clinical Trial Summary

This is a prospective observational study aiming to evaluate the diagnostic accuracy of the high-sensitivity Troponin assay performed with the Atellica VTLi POCT system (by comparison with the results obtained with the Atellica diagnostic system currently in use) and to evaluate the impact of the POCT system on the reduction of decision-making time (particularly of "rule-out"), by evaluating the number of cases in which the conclusion of the decision pathway at 3 h (algorithm currently in use) could have been concluded at 1 h.

Clinical Trial Description

Patients accessing the emergency room for chest pain suspected of acute myocardial ischemia, who are asked for Troponin determination for the decision pathway, will be asked to participate at the study. A blood draw will be performed (for determination of Troponin value, with classical method in use and with POCT method) at time: - Zero (acess at the emergency room) - 1 h - 3 h ;

Study Design

Related Conditions & MeSH terms

NCT number NCT05764655
Study type Observational
Source Centro Cardiologico Monzino
Contact Maria Luisa Biondi, MD, PhD
Phone 02.58002292
Status Recruiting
Start date May 6, 2022
Completion date July 2023

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