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โ† Trials
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STICH-3.0 International Trial Consortium

RecruitingNAAges 18 Years - anyAllVastra Gotaland Region
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In plain words

What the trial is, and whether it could suit you

The primary objective of the STICH 3.0 Study is to determine whether CABG is superior to PCI in terms of all-cause mortality at 5 years in patients with severe CAD and iLVSD. Individual patient data from similar national RCTs independently powered for different efficacy endpoints will be pooled, harmonized, and analyzed. The primary endpoint is all-cause mortality.

Sign in to get the eligibility rules as simple questions to take to your doctor.

๐Ÿ“‹ Eligibility rules (as published)
Inclusion Criteria: * Age \>18 years * LVEF โ‰ค40% * Extensive coronary artery disease (typically defined as a British Cardiovascular Intervention Society jeopardy score of โ‰ฅ6, on a scale from 0 to 12, with higher scores indicating greater extent of disease). Exclusion Criteria: * Decompensated heart failure requiring inotropic/adrenergic support, invasive or non-invasive ventilation or intra-aortic balloon pump/ ventricular assist device therapy less than 48 hours prior to randomization; * Valvular heart disease or any other cardiac conditions (e.g. LV aneurysm) indicating the need for surgical repair/replacement; * Prohibitive bleeding risk or clinical scenario mandating avoidance of long-term dual antiplatelet therapy; * Pregnancy; * Circumstances likely to lead to poor treatment adherence; * STEMI within 72 hours; * PCI within 3 months.
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What it tests

  • Percutaneous Coronary Intervention (PCI)
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Where

1 site
Dep of Cardiology, Sahlgrenska University Hospital
Gothenburg, Sweden
๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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