Clinical Study to Validate the Use of a New Point of Care Troponin I Test

Status Active, not recruiting

Clinical Trial Summary

This trial is designed as a prospective, multi-center, observational study of "all-comers" eligible adult subjects presenting to participating emergency departments with symptoms suggestive of acute coronary syndrome (ACS)

Clinical Trial Description

This trial is designed as a prospective, multi-center, observational study of "all-comers" eligible adult subjects presenting to participating Emergency Departments (EDs) with symptoms suggestive of ACS and/or myocardial ischemia. Subjects presenting with symptoms suggestive of ACS will be screened and approached for consent for study enrollment by trained personnel.

After obtaining written informed consent, subjects will have up to 4 blood samples collected for cTnI testing using the Meritas Troponin I test and Meritas point-of-care (POC) Analyzer. Blood draws and testing will occur at 4 intervals over 24 hours. ;

Study Design

Time Perspective: Prospective

Related Conditions & MeSH terms

Acute Coronary Syndrome

Clinical Trial Details

NCT number	NCT02620397
Study type	Observational
Source	Trinity Biotech
Contact
Status	Active, not recruiting
Phase	N/A
Start date	March 2015
Completion date	November 2016

View Details

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