Overview

This trial is active, not recruiting.

Condition acute coronary syndrome
Sponsor Redmond Fire Department Medic One
Collaborator Medic One Foundation
Start date November 2006
End date November 2009
Trial size 1200 participants
Trial identifier NCT00764205, 20070224

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.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Observational model case control
Time perspective prospective
Arm
Troponin measured prior to hospital arrival
Patients transported to hospital without troponin measurements enroute

Primary Outcomes

Measure
Decrease door-to-reperfusion time for patients with non-STEMI's by measuring troponin levels prior to hospital arrival
time frame: 3-4 years

Eligibility Criteria

Male or female participants at least 18 years old.

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.

Additional Information

Official title Randomized Trial of Prehospital Troponin Assessment Using the i-STAT Blood Analyzer
Principal investigator James P Jordan, BS, MS, MICP
Trial information was received from ClinicalTrials.gov and was last updated in September 2008.
Information provided to ClinicalTrials.gov by Redmond Fire Department Medic One.