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Clinical Trials/NCT01435408
NCT01435408
Active, not recruiting
Not Applicable

A Randomised Comparison of the Clinical Outcome After Postconditioning or Deferred Stent Implantation Versus Conventional Treatment

Rigshospitalet, Denmark5 sites in 1 country2,000 target enrollmentApril 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
ST Segment Elevation Myocardial Infarction
Sponsor
Rigshospitalet, Denmark
Enrollment
2000
Locations
5
Primary Endpoint
All cause mortality, heart failure (postconditioning)
Status
Active, not recruiting
Last Updated
3 years ago

Overview

Brief Summary

This study focuses on Cardioprotective strategies.

Registry
clinicaltrials.gov
Start Date
April 2011
End Date
December 2024
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Thomas Engstrom

MD, DMSci, PhD

Rigshospitalet, Denmark

Eligibility Criteria

Inclusion Criteria

  • Age ≥ 18 years.
  • Acute onset of chest pain of \< 12 hours' duration.
  • ST-segment elevation ≥ 0.1 mV in ≥ 2 contiguous leads, signs of a true posterior infarction or documented newly developed left bundle branch block.
  • Culprit lesion in a major native vessel.

Exclusion Criteria

  • Pregnancy.
  • Known intolerance of ASA, clopidogrel, heparin or contrast.
  • Inability to understand information or to provide informed consent.
  • Haemorrhagic diathesis or known coagulopathy.
  • Stent thrombosis.

Outcomes

Primary Outcomes

All cause mortality, heart failure (postconditioning)

Time Frame: 2 years

Secondary Outcomes

  • All cause mortality, myocardial infarction, repeat revascularisation and occurrence of definite stent thrombosis according to ARC definition within 1 year (deferred stent strategy)(1 year)
  • Infarct size in relation to area at risk as determined by MRI after 3 month(3 month)

Study Sites (5)

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