Computed Tomography Coronary Angiogram (CTCA) Versus Traditional Care in Emergency Department Assessment of Potential Acute Coronary Syndromes (ACS)
Completed · Not applicable
Conditions studied: Chest Pain, Acute Coronary Syndrome, Acute Myocardial Infarction, Coronary Artery Disease
In brief
This multi-center, randomized, controlled trial conducted in Emergency Departments (ED) compares computed tomography (CT) coronary angiography with the traditional approach (usual care) for low- to intermediate-risk chest pain patients. The primary objective is to estimate the rate of major cardiac events (heart attack or cardiac death) within 30 days in trial participants in Group B who were not found to have significant coronary artery disease by CT coronary angiography. Additional evaluations will comprise health care utilization assessments, including length of hospital stay and re-admissions, cost analysis, and 1-year post-triage/presentation major cardiac event rates.
Key facts
- Study ID
- NCT00933400
- Run by
- American College of Radiology
- People needed
- 1392
- Starts
- 2009-07-01
- Expected to finish
- 2012-04-01
- Last updated by the study team
- 2024-03-06
Who can join
Age: 30 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Participant is 30 years of age or older
- Participant presents with complaints consistent with potential ACS (e.g., chest pain, shortness of breath, other)
- Participant requires admission or objective testing to exclude ACS
- Participant with initial ECG result without acute ischemia
- Participant with an initial Thrombolysis in Myocardial Infarction (TIMI) Risk Score of 0 to 2
- Participant is willing to provide a written informed consent
You may not qualify if…
- Patients who present with symptoms that are clearly not cardiac in origin (e.g., chest pain secondary to herpes zoster, obvious pneumonia, or recent trauma);
- Patients with no initial ECG performed in the ED
- Patients with ST-elevation myocardial infarction (STEMI)
- Patients with existing co-morbidity that requires admission regardless of presence of ACS (e.g., uncontrolled diabetes)
- Patients with known contraindications to CT coronary angiography: Iodinated contrast allergic-like reaction
- Patients who are known to have had CT coronary angiography in the year prior to presentation
- Patients who are known to have normal catheterization results (no or minimal, < 25%, stenosis) in the year prior to presentation
- Patients who are pregnant
- Patients with known renal insufficiency (e.g., creatinine clearance < 60 mL/min/1.73 m2)
- Patients with no telephone or cell phone numbers (preventing follow up)
- Patients unwilling to provide a written informed consent
Where it is running
- Wake Forest University Baptist Medical Center — Winston-Salem, North Carolina, United States
- Penn State Hershey - Milton S. Hershey Medical Center — Hershey, Pennsylvania, United States
- Penn-Presbyterian Medical Center — Philadelphia, Pennsylvania, United States
- University of Pennsylvania Health System — Philadelphia, Pennsylvania, United States
- University of Pittsburgh Medical Center — Pittsburgh, Pennsylvania, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.