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CompletedNCT07373678RITUALUpdated Jan 28, 2026

CABG Versus PCI in Patients With Isolated LAD Chronic Total Occlusion

An observational study in Chronic Total Occlusion, sponsored by Mersin Medicalpark Hastanesi. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-01-28.

Sponsored by Mersin Medicalpark Hastanesi · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
302
Ages
18 Years and older
Sex
All
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Study summary

The aim of this study is to compare coronary artery bypass grafting (CABG) and percutaneous coronary intervention (PCI) in the treatment of isolated chronic total occlusion (CTO) of the left anterior descending (LAD) artery in terms of short- and mid-term clinical outcomes, myocardial revascularization success, and complication rates.

Read the detailed description

Chronic total occlusion (CTO) represents one of the most challenging subgroups of coronary artery disease and is closely associated with adverse cardiovascular outcomes. Previous studies have demonstrated that patients with CTO experience a higher incidence of major adverse cardiovascular events compared with patients without CTO but with significant coronary artery disease (CAD), even after adjustment for demographic characteristics, clinical parameters, and disease severity. Among these patients, those with unrevascularized CTO constitute the highest-risk group, whereas successful revascularization has been shown to reduce the risk to a level comparable to that of patients without CTO but with significant CAD.

Among CTOs, isolated total occlusion of the left anterior descending (LAD) artery has particular clinical importance due to its critical role in myocardial perfusion. Two main revascularization strategies are currently used in the treatment of isolated LAD CTO: percutaneous coronary intervention (PCI) and single-vessel coronary artery bypass grafting (CABG). In surgical revascularization, the left internal mammary artery (LIMA) is most commonly used, although saphenous vein grafts may be preferred in selected cases.

However, direct comparative data between these two treatment strategies in this specific patient population remain extremely limited. In particular, differences between CTO-PCI and single-vessel CABG with respect to revascularization success, in-hospital events, and early post-discharge outcomes have not been systematically evaluated. In the present study, within the framework of the RITUAL study, the outcomes of CTO-PCI and CABG surgery were compared in patients with isolated LAD CTO.

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Conditions studied

  • Chronic Total Occlusion

Keywords

  • Chronic total occlusion
  • Coronary artery bypass
  • Percutaneous coronary intervention
  • left anterior descending artery
  • isolated LAD CTO
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In context

Lead sponsor

Mersin Medicalpark Hastanesi is the lead sponsor of 4 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

The study population consists of adult patients aged 18 years or older with isolated chronic total occlusion (CTO) of the left anterior descending (LAD) coronary artery who underwent coronary revascularization with either coronary artery bypass grafting (CABG) or percutaneous coronary intervention (PCI) as part of routine clinical care. Isolated LAD CTO was defined as a de novo or in-stent total occlusion confined to the LAD artery, without significant coronary artery disease (≥50% stenosis) in other major epicardial coronary arteries. Patients with prior coronary revascularization, multiple CTOs, severe left ventricular dysfunction, or incomplete follow-up data were excluded.

Inclusion criteria

  • Age 18 years or older at the time of the index procedure.
  • Diagnosis of isolated chronic total occlusion (CTO) of the left anterior descending (LAD) coronary artery.
  • Isolated LAD CTO defined as a de novo or in-stent total occlusion confined to the LAD artery, without significant coronary artery disease (defined as ≥50% stenosis) in other major epicardial coronary arteries, including the left circumflex (LCx), right coronary artery (RCA), or major side branches.
  • No prior percutaneous coronary intervention (PCI) performed in non-LAD coronary arteries.
  • Patients who underwent coronary revascularization with either coronary artery bypass grafting (CABG) or percutaneous coronary intervention (PCI) for isolated LAD CTO.

Exclusion criteria

Exclusion Criteria:

  • History of malignancy or active malignant disease at the time of the index procedure.
  • Prior coronary artery bypass grafting (CABG) or prior percutaneous coronary intervention (PCI) performed in non-LAD coronary arteries.
  • Presentation with ST-segment elevation myocardial infarction (STEMI).
  • Discontinuation of prescribed medical therapy by patient preference within one year after the index procedure.
  • Presence of multiple chronic total occlusions (CTOs) involving more than one coronary artery.
  • Significant side branch disease of the LAD requiring two bypass grafts.
  • Performance of crossover stenting from the LAD into the left main coronary artery during LAD CTO-PCI.
  • Treatment of LAD CTO with drug-eluting balloon (DEB) angioplasty without stent implantation.
  • Left ventricular ejection fraction (LVEF) less than 30%.
  • Presence of severe valvular heart disease (e.g., severe aortic or mitral stenosis or regurgitation).
  • Incomplete angiographic or clinical follow-up data.
  • Use of mechanical circulatory support devices due to advanced heart failure, including intra-aortic balloon pump (IABP), extracorporeal membrane oxygenation (ECMO), or left ventricular assist device (LVAD).
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Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
302 participants (actual)
Patient registry
No

Groups and cohorts

  • Coronary Artery Bypass Grafting (CABG)

    Patients with isolated chronic total occlusion of the left anterior descending artery who underwent coronary artery bypass graft surgery.

    Procedure: Coronary Artery Bypass Grafting

  • Percutaneous Coronary Intervention (PCI)

    Patients with isolated chronic total occlusion of the left anterior descending artery who underwent percutaneous coronary intervention.

    Procedure: Percutaneous Coronary Intervention

Interventions

  • ProcedureCoronary Artery Bypass Grafting

    Coronary artery bypass graft surgery performed as part of routine clinical care prior to study inclusion.

  • ProcedurePercutaneous Coronary Intervention

    Percutaneous coronary intervention performed as part of routine clinical care prior to study inclusion.

06

What researchers measure

Primary outcomes

  1. Procedural success

    Successful completion of coronary revascularization of the left anterior descending artery without in-hospital major adverse cardiac events.

    Time frame: perioperatively / periprocedurally

Secondary outcomes

  1. Major adverse cardiac events (MACCE) at 3 years

    Composite endpoint including all-cause mortality, non-fatal myocardial infarction, cerebrovascular events, and target vessel revascularization within 3 years after the index procedure.

    Time frame: 3 years

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Study locations

1 site
  • Sefa SURAL
    Mersin, 33010, Turkey (Türkiye)
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References and documents

Individual participant data

Plan to share: No — Individual participant data will not be shared due to the retrospective design of the study and institutional data privacy policies.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 28, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07373678
Lead sponsor
Mersin Medicalpark Hastanesi
Collaborators
Biruni University, Mersin Training and Research Hospital, Necmettin Erbakan University, Jolimont Hospital, Minneapolis Heart Institute
Responsible party
Sefa Sural (Assistant Professor of Cardiology, Mersin Medicalpark Hastanesi) — Principal investigator
First posted
Jan 28, 2026
Start date
Sep 10, 2025
Primary completion
Dec 31, 2025
Completion
Jan 15, 2026
Last update
Jan 28, 2026

Study contacts

Sefa SURAL, MD
principal investigator · Toros University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jan 2026. You cannot join it, but the record below documents what was studied.

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