Low Risk Acute Coronary Syndrome

Not Applicable

Completed

• Conditions: Low Risk Acute Coronary Syndrome

• Registration Number: NCT01703156
• Lead Sponsor: University of Oklahoma

Brief Summary

A large number of patients are diagnosed with low risk ACS, and these individuals are at significant cardiovascular risk. Though guidelines recommend stress testing to manage low risk ACS patients, evidence supporting this recommendation is not based on trials examining this population. A well-designed, randomized trial is warranted to determine if stress testing is useful in managing low risk ACS. If medical therapy alone is equivalent as the investigators hypothesize, healthcare expenditures could be reduced and patients may not be exposed to the harms associated with more invasive cardiac testing such as coronary angiography.

Detailed Description

Not available

Study Timeline

• Study Start: 2009-05
• Primary Completion: 2012-07
• Study Completion: 2012-07
• Study First Submitted: 2012-10-03
• Study First Submitted QC: 2012-10-09
• Study First Posted: 2012-10-10
• Status Verified: 2017-04
• Last Update Submitted: 2017-04-10
• Last Update Posted: 2017-04-12

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 70

Inclusion Criteria

1. TIMI score < or = to 2(12)
2. TIMI risk score of 3 with no known CAD, greater than 50% in one or more vessels
3. Normal cardiac biomarkers (3 sets over 12-88 hours)
4. No evidence of acute ischemia on electrocardiograms
5. Normal ejection fraction (>40%) on echocardiography
6. Age 30-75
7. Ability to complete noninvasive stress test
8. Ability to provide informed consent

Exclusion Criteria

1. Presence of another medical condition to explain chest pain or non-cardiac chest pain (i.e. pneumonia, costochondritis)
2. Any patient who is initially classified as low risk but whom develops recurrent symptoms of ischemia, hemodynamic instability, or arrhythmias attributable to ischemia
3. Evidence of ischemia on electrocardiogram
4. Abnormal cardiac biomarkers
5. History of medical noncompliance or social circumstances preventing compliance
6. Life span estimated at <1 year
7. Pregnancy
8. Refusal to sign consent

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Composite of all-cause mortality, hospitalization for UA/NSTEMI or STEMI, and urgent revascularization	one year	Primary endpoints include the composite of all-cause mortality, hospitalization for Unstable Angina/Non ST-Elevation Myocardial Infarction (UA/NSTEMI) or ST-Elevation Myocardial Infarction (STEMI), and urgent revascularization (coronary artery bypass grafting or percutaneous coronary intervention).

Secondary Outcome Measures

Name	Time	Method
Secondary endpoints will include mortality, UA/NSTEMI or STEMI, coronary revascularization, unplanned diagnostic coronary angiography, noninvasive stress testing, medication adjustments, and medication side effects.	one year	Secondary endpoints will include: mortality, UA/NSTEMI or STEMI, coronary revascularization, unplanned diagnostic coronary angiography, noninvasive stress testing, medication adjustments, and medication side effects.

Trial Locations

Locations (1)

Veteran's Affairs Medical Center; 🇺🇸 Oklahoma City, Oklahoma, United States