Status:
COMPLETED
Myeloperoxidase and Multi-Markers In the Diagnosis of Diagnoses of Acute Coronary Syndrome (MIDAS) - Sample Procurement
Lead Sponsor:
Abbott RDx Cardiometabolic
Conditions:
Acute Coronary Syndrome (ACS)
Eligibility:
All Genders
18+ years
Brief Summary
The purpose of the study is to procure blood samples from patients who present to the Emergency Department with suspected ACS (Acute Coronary Syndrome).
Detailed Description
This is a prospective, multi-center, observational, and sample procurement study of adult subjects presenting to an Emergency Department (ED) in whom ACS is in the differential diagnosis. Subjects mus...
Eligibility Criteria
Inclusion
- Age 18 years or older at time of enrollment
- Patient presenting to the ED within 6 hours or less from symptom (chest discomfort consistent with possible ACS) onset
- Patient experiencing at least 30 minutes of chest discomfort, consistent with possible ACS, from time of symptom onset; patients who have symptoms of shorter duration due to pharmacologic intervention may be included
- Physician plans to perform objective cardiac testing as defined by the protocol
Exclusion
- Patient (or legal representative) unable or unwilling to provide informed consent
- Patient (or legal representative) refusal of medical record review or telephone follow-up at 30 days or 6 months
- Patient (or legal representative) refusal of multiple blood sample collection over the study period
- Prisoners or other institutionalized individuals
Key Trial Info
Start Date :
December 1 2006
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
June 1 2008
Estimated Enrollment :
300 Patients enrolled
Trial Details
Trial ID
NCT00415948
Start Date
December 1 2006
End Date
June 1 2008
Last Update
December 18 2009
Active Locations (18)
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1
UC Davis
Sacramento, California, United States
2
Yale University
New Haven, Connecticut, United States
3
St Agnes Hospital
Baltimore, Maryland, United States
4
Beth Israel Deaconess Medical Center
Boston, Massachusetts, United States