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NCT06899776 · ClinicalTrials.gov registry record
Assessing Chest Pain Using Point-of-Care High-Sensitivity Troponin I in the Emergency Department
A clinical trial of ACS (Acute Coronary Syndrome), sponsored by Wake Forest University Health Sciences.
- Active
- Registry status
- 600
- Enrollment target
- 3
- Study locations
NCT06899776 is a study of ACS (Acute Coronary Syndrome) that is active but no longer recruiting, run by Wake Forest University Health Sciences. The registered enrollment target is 600 participants. The trial reports 3 study locations across 1 state.
The verdict
NCT06899776, a study of ACS (Acute Coronary Syndrome), is active but no longer recruiting, sponsored by Wake Forest University Health Sciences.
- ACTIVE NOT RECRUITING
- Registry status
- 600 participants
- Enrollment target
- 3
- Study locations
Study Summary
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.
Conditions Studied
Interventions
- DEVICE Abbott i-STAT point of care (POC) device
Study Locations (3)
North Carolina
- Carolinas Medical Center - Charlotte
- High Point Medical Center - High Point
- Wake Forest School of Medicine - Winston-Salem
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 600 participants |
| Start Date | 2025-02-07 |
| Est. Completion | 2026-07 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06899776
The ClinicalTrials.gov registry entry for NCT06899776 describes a study currently listed as active not recruiting, categorized as an unspecified phase. The registered enrollment target is 600 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Wake Forest University Health Sciences, which has 1,140 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with ACS (Acute Coronary Syndrome) appearing as the primary indexed condition, and to 1 intervention - of which Abbott i-STAT point of care (POC) device is the first listed.
NCT06899776 reports 3 study locations spanning 1 distinct geographic area - top geographies include North Carolina.
Frequently Asked Questions
What is clinical trial NCT06899776 about?
NCT06899776 is a clinical study titled "Assessing Chest Pain Using Point-of-Care High-Sensitivity Troponin I in the Emergency Department". 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 in...
What is the current status of trial NCT06899776?
This trial is currently active not recruiting. The enrollment target is 600 participants. The study started on 2025-02-07. Estimated completion is 2026-07.
What conditions does trial NCT06899776 study?
This clinical trial studies the following conditions: ACS (Acute Coronary Syndrome).
What interventions are being tested in trial NCT06899776?
The interventions under investigation include: Abbott i-STAT point of care (POC) device (DEVICE).
Who is sponsoring clinical trial NCT06899776?
This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06899776 being conducted?
This trial has 3 study locations across North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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