🏛️ Verified NIH Record • Updated 2026-04-27

The Canadian CABG or PCI in Patients With Ischemic Cardiomyopathy Trial (STICH3C) (NCT05427370)

The Canadian CABG or PCI in Patients With Ischemic Cardiomyopathy Trial

🟢 Recruiting Observational / Diagnostic 🩺 Clinical Procedure Protocol Sponsor: Sunnybrook Health Sciences Centre

🩺 Plain-English Summary (8th-Grade Level)

The Canadian CABG or PCI in Patients With Ischemic Cardiomyopathy (STICH3C) trial is a prospective, unblinded, international multi-center randomized trial of 754 subjects enrolled in approximately 45 centers comparing revascularization by percutaneous coronary intervention (PCI) vs. coronary artery bypass grafting (CABG) in patients with multivessel/left main (LM) coronary artery disease (CAD) and reduced left ventricular ejection fraction (LVEF). The primary objective is to determine whether CABG compared to PCI is associated with a reduction in all-cause death, stroke, spontaneous myocardial infarction (MI), urgent repeat revascularization (RR), or heart failure (HF) readmission over a median follow-up of 5 years in patients with multivessel/LM CAD and ischemic left ventricular dysfunction (iLVSD). Eligible patients are considered by the local Heart Team appropriate and amenable for non-emergent revascularization by both modes of revascularization. The secondary objectives are to describe the early risks of both procedures, and a comprehensive set of patient-reported outcomes longitudinally.

Who can join: Review the eligibility criteria below.

Location: Cedars-Sinai — Los Angeles, California

Age range: 18 Years

🧪 Interventions in This Study

  • Revascularization by PCI (PROCEDURE)
  • Revascularization by CABG (PROCEDURE)

📋 "Do I Qualify?" — 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria ↗

📍 All Participating Trial Locations (43 Sites)

Showing the first 25 of 43 sites.

  • Cedars-Sinai — Los Angeles, California
  • Yale University — New Haven, Connecticut
  • UofL Health, Inc — Louisville, Kentucky
  • John Hopkins Hospital — Baltimore, Maryland
  • Mayo Clinic — Rochester, Minnesota
  • University Hospitals Cleveland Medical Center — Cleveland, Ohio
  • Medical University of Vienna — Vienna,
  • Heart Institute, Medical School of the University of Sao Paulo_INCOR — São Paulo,
  • University of Calgary; Libin Cardiovascular Institute — Calgary, Alberta
  • Mackenzie Health Sciences Center — Edmonton, Alberta
  • Fraser Health; Royal Columbian Hospital — New Westminster, British Columbia
  • Providence Health — Vancouver, British Columbia
  • The University of Manitoba and St. Boniface Hospital Inc. — Winnipeg, Manitoba
  • Queen Elizabeth II Hospital — Halifax, Nova Scotia
  • Hamilton General Hospital — Hamilton, Ontario
  • London Health Sciences Center, University Hospital — London, Ontario
  • Southlake Regional HC — Newmarket, Ontario
  • Ottawa Heart Institute — Ottawa, Ontario
  • Sunnybrook Health Sciences Center — Toronto, Ontario
  • St. Michael's — Toronto, Ontario
  • Toronto General Hospital — Toronto, Ontario
  • Center Hospitalier Universitaire de Montreal — Montreal, Quebec
  • Montreal Heart Institute — Montreal, Quebec
  • Hospital Sacre-Coeur — Montreal, Quebec
  • Institut de Cardiologie Quebec (QC) - Laval — Québec, Quebec

📞 Contact the Study Coordinator

Phone: (416) 480-6100

Email: stephen.fremes@sunnybrook.ca

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

💰 Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

💡 How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
🏛️ View Official NIH Record ↗