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

Conditions
Acute Coronary Syndrome
Registration Number
NCT00764205
Lead Sponsor
Redmond Fire Department Medic One
Brief 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.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
1200
Inclusion Criteria
  • Over years of age
  • ACS without ST-segment elevation
  • Patient being transported to one of two participating hospitals
Exclusion Criteria
  • Less then 18 years of age.
  • Post cardiac arrest.
  • ACS with ST-segment elevation.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Decrease door-to-reperfusion time for patients with non-STEMI's by measuring troponin levels prior to hospital arrival3-4 years
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Redmond Fire Department Medic One Units

🇺🇸

-Mobile Units in King County-, Washington, United States

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