NCT01435408
Active, not recruiting
Not Applicable
A Randomised Comparison of the Clinical Outcome After Postconditioning or Deferred Stent Implantation Versus Conventional Treatment
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.
Investigators
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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