Evaluation of Serial Troponin and Cardiac Multimarkers at the Point of Care in the Emergency Department

Status

Withdrawn

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT00907231

Acronym

ESTIMATE

Enrollment

Registered

2009-05-22

Start date

2010-02-28

Completion date

2010-05-31

Last updated

2015-07-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Coronary Syndrome, Acute Myocardial Infarction, Chest Pain

Brief summary

This is a multi-center study to assess the diagnostic accuracy of the Troponin I assay in the Biosite Triage Cardio3 Panel at the point-of-care (POC) in adults presenting to the emergency department with possible acute myocardial infarction (AMI).

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

* 18 years of age or older at time of enrollment * Presenting to the ED within 6 hours from onset of chest discomfort (pain, pressure, tightness, etc) consistent with a possible diagnosis of AMI or ACS and with an initial ECG non-diagnostic for injury (or injury equivalent resulting in emergent reperfusion therapy). (NOTE: Subjects who have chest discomfort that is episodic or stuttering in nature may be included if the ED presentation is within 6 hours of symptom onset.) * Experiencing at least 30 minutes of chest pain or other anginal equivalent symptoms. (Note: Subjects who have symptoms of shorter duration due to pharmacologic intervention may be included.)

Exclusion criteria

* Patient (or Legal Representative) unable or unwilling to provide written informed consent. * Patient unwilling or unlikely to comply with study procedures, including protocol-specified blood sampling or telephone follow-up at 30 days and 6 months. * Vulnerable populations as deemed inappropriate for study by site principal investigator. * ST-elevation or other ECG criteria that result that is diagnostic for AMI and results in patient being sent for percutaneous coronary interventions (PCI) or being treated with thrombolytics6. * Pulmonary Edema requiring CPAP, BIPAP, or mechanical ventilation * Tachyarrhythmias (SVT, V-Tach, rapid atrial fib) * End Stage Renal Disease on Hemodialysis * Cardiac Arrest prior to arrival * Implantable Defibrillator firing prior to arrival * Hemodynamically unstable patients * Trauma injury to the chest

Countries

United States

Outcome results