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Randomized Trial of Prehospital Tropin Levels in Acute Coronary Syndrome (ACS)

NCT00764205 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 1200

Last updated 2008-10-01

No results posted yet for this study

Summary

This study randomizes patients seen by Redmond Medic One into a control arm and a study arm when they present with acute coronary syndrome and have non-contributory ECG's (i.e.non-STEMI). The control group is treated normally and delivered to the receiving hospital. The study group is treated normally as well, however troponin measurements are made using an i-STAT blood analyzer prior to hospital arrival. The results are presented to the receiving physician. Door-to-reperfusion time is monitored for both groups.

Conditions

  • Acute Coronary Syndrome

Sponsors & Collaborators

  • Medic One Foundation

    collaborator OTHER

  • Redmond Fire Department Medic One

    lead OTHER_GOV

Principal Investigators

  • James P Jordan, BS, MS, MICP · Redmond Fire Department Medic One

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-11-30
Primary Completion
2009-11-30
Completion
2010-11-30

Countries

  • United States

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00764205 on ClinicalTrials.gov