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Clinical Trial Details — Status: Unknown status

Administrative data

NCT number NCT00161005
Other study ID # 2935-0304 (UUS)
Secondary ID 2004-162 (Helse
Status Unknown status
Phase N/A
First received September 9, 2005
Last updated April 16, 2009
Start date February 2005
Est. completion date December 2009

Study information

Verified date April 2009
Source Ullevaal University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Unknown status
Enrollment 266
Est. completion date December 2009
Est. primary completion date June 2009
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
PCI
Immediate transport to invasive center after thrombolysis

Locations

Country Name City State
Norway Ulleval University Hospital Oslo

Sponsors (2)

Lead Sponsor Collaborator
Ullevaal University Hospital Helse Innlandet

Country where clinical trial is conducted

Norway, 

Outcome

Type Measure Description Time frame Safety issue
Primary Death , myocardial infarction ,stroke or ischemia during 12 months. 12 months
Primary Costs during 12 months. 12 months
Secondary Size of infarction. 3 months
Secondary Complications 1 month
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