NCT00764205

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.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
1,200

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Nov 2006

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 1, 2006

Completed
1.9 years until next milestone

First Submitted

Initial submission to the registry

September 30, 2008

Completed
1 day until next milestone

First Posted

Study publicly available on registry

October 1, 2008

Completed
1.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2009

Completed
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2010

Completed
Last Updated

October 1, 2008

Status Verified

September 1, 2008

Enrollment Period

3 years

First QC Date

September 30, 2008

Last Update Submit

September 30, 2008

Conditions

Keywords

ACSnon STEMIECG troponiniSTATAcute coronary syndrome without ST-segment elevation

Outcome Measures

Primary Outcomes (1)

  • Decrease door-to-reperfusion time for patients with non-STEMI's by measuring troponin levels prior to hospital arrival

    3-4 years

Study Arms (2)

Study Group

Troponin measured prior to hospital arrival

Control Group

Patients transported to hospital without troponin measurements enroute

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients seen and treated by Redmond Fire Department Medic One.

You may qualify if:

  • Over years of age
  • ACS without ST-segment elevation
  • Patient being transported to one of two participating hospitals

You may not qualify if:

  • Less then 18 years of age.
  • Post cardiac arrest.
  • ACS with ST-segment elevation.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Redmond Fire Department Medic One Units

-Mobile Units in King County-, Washington, 98052, United States

Location

MeSH Terms

Conditions

Acute Coronary SyndromeNon-ST Elevated Myocardial Infarction

Condition Hierarchy (Ancestors)

Myocardial IschemiaHeart DiseasesCardiovascular DiseasesVascular DiseasesMyocardial InfarctionInfarctionIschemiaPathologic ProcessesPathological Conditions, Signs and SymptomsNecrosis

Study Officials

  • James P Jordan, BS, MS, MICP

    Redmond Fire Department Medic One

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER GOV

Study Record Dates

First Submitted

September 30, 2008

First Posted

October 1, 2008

Study Start

November 1, 2006

Primary Completion

November 1, 2009

Study Completion

November 1, 2010

Last Updated

October 1, 2008

Record last verified: 2008-09

Locations