Clinical and Economic Outcomes of High Sensitivity Troponin for no ST Elevation Myocardial Infarction in Patients With Chest Pain in Emergency Departments in Italy-An Observational Study

NCT03489603 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 2913

Last updated 2021-02-26

No results posted yet for this study

Summary

Myocardial infarction is one of the leading causes of death and disability worldwide. In addition to standard diagnostic methods, it has been shown that high-sensitivity cardiac troponin assays allow greater sensitivity in the diagnosis of myocardial infarction and assume a central role for both exclusion ("rule out") and confirmation ("rule in") of acute myocardial infarction , while allowing to reduce the time interval between ER admission and presumptive diagnosis.

Considering the relevance of this topic, we propose to conduct an observational study in real world clinical practice settings at Emergency Departments, aiming to evaluate clinical and economic aspects deriving from the use of the different quantitative assays of high-sensitivity cardiac troponin currently available in patients with suspected acute myocardial infarction and non-ST-elevation ECG (NSTEMI) on the admission, including time of diagnosis and number of laboratory and imaging tests performed.

Conditions

  • NSTEMI - Non-ST Segment Elevation MI

Sponsors & Collaborators

  • Azienda Ospedaliero Universitaria Maggiore della Carita

    collaborator OTHER
  • Azienda Sanitaria Locale ASL 6, Livorno

    collaborator OTHER_GOV
  • Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia

    collaborator OTHER
  • Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico

    collaborator OTHER
  • Ospedale Civile - Padova

    collaborator UNKNOWN
  • S. Andrea Hospital

    collaborator OTHER
  • Azienda Policlinico Umberto I

    collaborator OTHER
  • San Carlo Public Hospital, Potenza, Italy

    collaborator OTHER
  • Azienda Ospedaliero-Universitaria Consorziale Policlinico di Bari

    collaborator OTHER
  • Policlinico Universitario, Catania

    collaborator OTHER
  • Azienda Ospedaliera Sant'Anna

    collaborator OTHER
  • Ospedale di Cattinara - Azienda Universitaria Integrata -Trieste

    collaborator UNKNOWN
  • Abbott

    collaborator INDUSTRY
  • Informapro Srl

    collaborator OTHER
  • Marco Marchetti

    lead OTHER

Principal Investigators

  • Marco Marchetti, MD · Istituto Superiore di Sanità

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-10-11
Primary Completion
2018-07-11
Completion
2019-06-15

Countries

  • Italy

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03489603 on ClinicalTrials.gov