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NCT00764205 Clinical Trial

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

Acute Coronary Syndrome Clinical Trial

Official title:
Randomized Trial of Prehospital Troponin Assessment Using the i-STAT Blood Analyzer

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT00764205
Other study ID # 20070224
Secondary ID
Status Active, not recruiting
Phase N/A
First received September 30, 2008
Last updated September 30, 2008
Start date November 2006
Est. completion date November 2010

Study information
Verified date September 2008
Source Redmond Fire Department Medic One
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial 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.

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 1200
Est. completion date November 2010
Est. primary completion date November 2009
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility 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

Observational Model: Case Control, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
United States Redmond Fire Department Medic One Units -Mobile Units in King County- Washington

Sponsors (2)
Lead Sponsor Collaborator
Redmond Fire Department Medic One Medic One Foundation

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Decrease door-to-reperfusion time for patients with non-STEMI's by measuring troponin levels prior to hospital arrival 3-4 years No
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