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Improving Door-to-Balloon Time in STEMI (EHART)

S

St. Francis Hospitals & Health Centers

Status

Unknown

Conditions

Myocardial Infarction

Treatments

Other: ED Activation/Immediate Transfer

Study type

Interventional

Funder types

Other

Identifiers

NCT00800163
St. Francis Heart Center-EHART

Details and patient eligibility

About

The investigators prospectively determined the impact on median door-to-balloon time of a protocol mandating (1) emergency department physician activation of the catheterization lab and (2) immediate transfer of the patient to an immediately available catheterization lab by an in-house transfer team consisting of an emergency department nurse, a critical care unit nurse, and a chest pain unit nurse.

Full description

Please see Circulation. 2007;116:67-76

Enrollment

1,000 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Primary Study Inclusion Criteria:

  • ST-elevation myocardial infarction patients who undergo percutaneous intervention within 24 hours of ED arrival

Exclusion Criteria:

  • Patients who are inpatients

A registry of all patients who undergo emergency cardiac catheterization irrespective of etiology is maintained.

Trial design

1,000 participants in 1 patient group

ED Physician Activation/Immediate Transfer
Experimental group
Treatment:
Other: ED Activation/Immediate Transfer

Trial contacts and locations

1

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Central trial contact

Umesh N Khot, M.D.; Michele Johnson-Wood, R.N

Data sourced from clinicaltrials.gov

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