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NCT Number: NCT05534698

Coronary Artery Bypass Grafts or Percutaneous Coronary Intervention for High Risk Patients

Most patients with Left Ventricular Systolic Dysfunction (LVSD) or heart failure (HF) have coronary artery disease (CAD) while some patients also have renal disease. Life-saving revascularization is underperformed in patients with LVSD or HF due to CAD, and especially if there is concomitant renal disease. We hypothesize that PCI will be non-inferior to CABG for all-cause mortality and recurrent myocardial infarction (MI), stroke or hospitalization for HF. To compare revascularization by PCI versus by CABG, we will perform a multicentre, open-label, parallel, randomized, controlled trial in patients with severe CAD who belong to defined categories of moderate-to-high risk characteristics, where guidelines acknowledge that both PCI and CABG are relevant treatment options.

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Key information

Age range

18 year–100 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Rigshospitalet, University of Copenhagen

Copenhagen, 2100, Denmark

Location contact

Lars Køber, MD, D.Sci

CONTACT

[email protected]

35 45 33 76

About this study

The STICH trial demonstrated a reduction in overall mortality after 10 years, but the 5-year analyses did not show significant benefits of CABG versus medical therapy. The extension of the STICH study, the STICHES study established the superiority of CABG over medical therapy for all-cause mortality (58.9% versus 66.1%; HR 0.84, 95%CI: 0.73-0.97; p = 0.02) over 9.8 years. Thus, these studies suggest that to offset the early operative risks of CABG, 10-year survival is needed. As many patients with HF and/or LVSD are elderly, both clinicians and patients are often unwilling to accept increased short-term risk even if they might eventually achieve long-term benefit, and thus not favour CABG. The available evidence suggest that PCI is feasible for patients with ischemic LVSD, and that PCI may yield long-term mortality rates like CABG with lower short-term morbidity The planned trial is a multicentre, open-label, parallel, randomized, controlled trial comparing revascularization by CABG versus by PCI in patients with severe CAD and at high risk, where guidelines accept both CABG and PCI as suitableand mortality. High risk is defined as patients with LVEF <45%, (irrespectively of clinical HF and severe renal disease), left anterior descending (LAD) disease in one- or two vessel disease, three-vessel disease with a SYNTAX score of up to 22 and left main disease with a SYNTAX score of up to 32.

The trial is powered for non-inferiorty.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥ 18 years
  • LVEF<45% with or without HF medication
  • Heart team believes that a meaningful revascularization can be achieve both by PCI and by CABG
  • Patients with severe CAD, where guidelines suggest equipoise between PCI and CABG

Exclusion criteria

  • Decompensated HF 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
  • Recent (< 1 month) ST-elevation myocardial infarction
  • Recent (< 1 month) type 2 myocardial infarction ▪ Valvular heart disease or any other cardiac conditions (for example, left ventricular aneurysm) indicating the need for surgical repair/replacement
  • Prohibitive bleeding risk or clinical scenario mandating avoidance of long-term dual antiplatelet therapy
  • Pregnancy

Treatment and study plan

PCI

Procedure

Revascularization by PCI

CABG

Procedure

Revascularization by CABG

Primary outcomes

  1. Composite of all-cause mortality, stroke, MI and hospitalization for HF

    Time frame: up to 10 years with analysis after 5 years

    time to event

Secondary outcomes

  1. Composite of occurrence of cardiovascular death or cardiovascular rehospitalization.

    Time frame: up to 10 years with analysis after 5 years

    time to event

Other outcomes

  1. combined occurrence of major bleeding, new renal filtration and dialysis

    Time frame: up to 10 years with analysis after 5 years

    Safety

Study contacts

Contact information is provided by the study sponsor or research team.

Lars V Køber, MD

CONTACT

[email protected]

31120540

Sponsors and collaborators

Lead sponsor

Danish Study Group

Network

Registry information

Official study title

Coronary Artery Bypass Grafts or Percutaneous Coronary Intervention for Revascularization in Moderate to Highs Risk Patients With Ischemic Heart Disease and Reduced Left Ventricular Ejection Fraction

Important dates

Study start
2022
Primary completion
2032
Study completion
2033
First posted
Sep 9, 2022
Registry last updated
Sep 15, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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