Coronary Artery Disease Clinical Trial
Official title:
Reduction in Infarct Size by Remote Per-postconditioning in Patients With ST-elevation Myocardial Infarction in Stockholm (RECOND)
- Trial objective: To test the hypothesis that remote per-postconditioning in connection
with primary PCI will reduce myocardial infarct size patients with STEMI.
- Trial Design: Placebo controlled randomized study with parallel groups
- Primary Endpoint: Myocardial infarct size expressed as a percentage of the myocardium
at risk determined by Cardiac Magnetic Resonance (CMR) day 4-7
- Efficacy Parameters: Myocardial infarct size expressed as a percentage to the
myocardium at risk determined by CMR at 6 months.
- Global left ventricular function determined by left ventricular ejection fraction
determined by CMR.
- Microvascular obstruction determined by CMR day 4-7. Quantified ECV (extracellular
volume) in left ventricular as myocardium at risk day 4-7 and remodelling parameters
day 180.
- Safety Parameters: Major adverse cardiovascular events.
See above. 3 patients left to include. ;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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