Are Serial Electrocardiograms Additive to SeriAl Second-generations Troponins in Predicting Acute CoronAry Syndromes in PatienTs With Undifferentiated cHest Pain
NCT ID: NCT01953276
Last Updated: 2022-02-17
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
382 participants
OBSERVATIONAL
2013-01-31
2018-01-15
Brief Summary
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Detailed Description
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Objective:
The goal of this project is to produce preliminary data to investigate whether the presence or absence of serial ECG changes suggestive of myocardial ischemia aids in reclassifying participants' risk for MACE and objective evidence of ACS over and above serial second-generation troponin testing.
Methods:
Adult patients, over 21 years old, presenting to WFBMC ED with chest pain or symptoms concerning for ACS, in which the provider orders cardiac biomarkers and an ECG will be eligible for enrollment. We aim to add serial ECG analysis (one at the time of study enrollment and a second at the time of the study blood draw) to the protocol in the proposed study. The primary outcomes are major adverse cardiovascular events (MACE) at 30 days and evidence of acute myocardial ischemia via objective cardiac testing performed during the index hospitalization.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Serial Electrocardiogram Arm
All study participants will receive serial electrocardiograms.
Serial Electrocardiograms
All participants will have serial electrocardiograms performed.
Interventions
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Serial Electrocardiograms
All participants will have serial electrocardiograms performed.
Eligibility Criteria
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Inclusion Criteria
* Chest discomfort or other symptoms consistent with possible ACS as indicated by the treating physician after obtaining an ECG and cardiac biomarkers for the patient's evaluation
* The treating physician feels the patient could be discharged home if cardiac disease was excluded
Exclusion Criteria
* Left ventricular systolic dysfunction (history of left ventricular ejection fraction \<40% or active symptoms of congestive heart failure)
* New or uncontrolled ventricular arrhythmias on initial ECG
* Hemodynamic instability: heart rate \> 120 bpm or \< 40 bpm and/or systolic blood pressure \<100 mmHg
* Hypoxemia (oxygen saturation \<90% on room air or normal home oxygen flow rate)
* Terminal diagnosis with life expectancy less than 1 year
* A non-cardiac medical, surgical, or psychiatric illness determined by the provider to require admission, increase risk of objective cardiac testing, or prevent immediate discharge following negative testing.
* Prior enrollment
* Incapacity or unwillingness to provide consent and comply with study procedures
21 Years
ALL
No
Sponsors
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American Heart Association
OTHER
Wake Forest University Health Sciences
OTHER
Responsible Party
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Principal Investigators
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Simon Mahler, MD
Role: PRINCIPAL_INVESTIGATOR
Wake Forest University Health Sciences
Locations
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Wake Forest University Baptist Medical Center - Emergency Department
Winston-Salem, North Carolina, United States
Countries
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References
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Other Identifiers
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IRB00022288
Identifier Type: -
Identifier Source: org_study_id
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