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Study identifier: NCT05761067 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

STICH-3.0 International Trial Consortium

Condition: Coronary Artery Disease · Heart Failure  ·  Sponsor: Vastra Gotaland Region

PhaseNA
Planned participants2800
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Björn Redfors, MD, PhD  ·  +46 313421000  ·  bjorn.redfors@wlab.gu.se

Mark Petrie, MD, PhD, Professor  ·  +44 141 330 4558  ·  Mark.Petrie@glasgow.ac.uk

Always discuss trial participation with your own doctor first.

Locations (1)

Dep of Cardiology, Sahlgrenska University HospitalGothenburg, SwedenRecruiting

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Source record: clinicaltrials.gov/study/NCT05761067