Assessing Chest Pain Using Point-of-Care High-Sensitivity Troponin I in the Emergency Department

Running, not enrolling

Conditions studied: ACS (Acute Coronary Syndrome)

In brief

The goal of this proposal is to improve the quality and value of care for patients with acute chest pain by investigating the potential impact of point-of-care (POC) high sensitivity cardiac troponin (hs-cTn) testing in the Emergency Department (ED) and exploring how best to integrate POC hs-cTnl into ED risk stratification workflows. The study hypothesizes that the Abbott i-STAT POC hs-cTnI assay will decrease time-to-result (TTR) and ED length of stay (LOS), while increasing ED revenue for patients with acute chest pain compared to a strategy of central laboratory hs-cTnI testing.

Key facts

Study ID
NCT06899776
Run by
Wake Forest University Health Sciences
People needed
600
Starts
2025-02-07
Expected to finish
2026-12-01
Last updated by the study team
2026-07-29

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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