Norwegian Study on District Treatment of ST-Elevation Myocardial Infarction

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

266 participants

Study Classification

INTERVENTIONAL

Study Start Date

2005-02-28

Study Completion Date

2009-12-31

Brief Summary

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In the district areas of Norway patients with acute myocardial infarction with ST-elevation, are treated with thrombolysis. An increasing part of them receives thrombolysis before arrival to the local hospital.Usually these patients have been sent to an invasive center if thrombolysis fails or the patient gets ischemic symptoms during the stay.

This study will compare this strategy against immediate transportation to an invasive center after the patient has received thrombolysis.

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Detailed Description

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Conditions

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Acute Myocardial Infarction

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Interventions

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PCI

Immediate transport to invasive center after thrombolysis

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Duration of painless than 6 hours.
* ST-segment elevation of at least 0.1 mV in two or more extremity leads or at least 0.2 mV in two or more precordial leads.
* The patient is getting thrombolysis.
* Time to reach an invasive center is more than 1 hour.
* Age 18-75 years.

Exclusion Criteria

* Known serious renal failure (creatinin \> 250 mmol/l)
* Pregnancy
* Cardiogenic chock
* Life threatening arrythmias
* Other serious diseases with life expectancy less than 1 year.
* Inability to perform an informed consent

Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No