Clinical trial

Diagnosis and Treatment of ACS in the ED: The Impact of Rapid Bedside cTnI…

NCT00222352 · University of Cincinnati, Other · Completed

Key facts

NCT number NCT00222352
Title Diagnosis and Treatment of ACS in the ED: The Impact of Rapid Bedside cTnI Testing on Outcomes
Official title Diagnosis and Treatment of Acute Coronary Syndromes in the Emergency Department: The Impact of Rapid Bedside cTnI Testing on Outcomes
Acronym Dispo-ACS
Lead sponsor University of Cincinnati, Other
Collaborators Abbott Industry Jewish Hospital, Cincinnati, Ohio University of Pennsylvania Stanford University Mayo Clinic
Status Completed
Study type Observational
Conditions Angina, Unstable
Intervention type Diagnostic Test
Interventions Point of Care cTnL testing
Enrollment 2,000
Start date Dec 1, 2004
Primary completion Nov 1, 2006
Completion Mar 1, 2007
First posted Sep 22, 2005
Last update posted Feb 5, 2018
Countries United States

At a glance

  • 1–9 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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