NCT07373678

Brief 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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
302

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Sep 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 10, 2025

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2025

Completed
15 days until next milestone

Study Completion

Last participant's last visit for all outcomes

January 15, 2026

Completed
2 days until next milestone

First Submitted

Initial submission to the registry

January 17, 2026

Completed
11 days until next milestone

First Posted

Study publicly available on registry

January 28, 2026

Completed
Last Updated

January 28, 2026

Status Verified

January 1, 2026

Enrollment Period

4 months

First QC Date

January 17, 2026

Last Update Submit

January 23, 2026

Conditions

Keywords

Chronic total occlusionCoronary artery bypassPercutaneous coronary interventionleft anterior descending arteryisolated LAD CTO

Outcome Measures

Primary Outcomes (1)

  • Procedural success

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

    perioperatively / periprocedurally

Secondary Outcomes (1)

  • Major adverse cardiac events (MACCE) at 3 years

    3 years

Study Arms (2)

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

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

Coronary Artery Bypass Grafting (CABG)

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

Percutaneous Coronary Intervention (PCI)

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-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.

You may qualify if:

  • 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.

You may not qualify if:

  • 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).

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Sefa SURAL

Mersin, 33010, Turkey (Türkiye)

Location

MeSH Terms

Interventions

Coronary Artery BypassPercutaneous Coronary Intervention

Intervention Hierarchy (Ancestors)

Myocardial RevascularizationCardiac Surgical ProceduresCardiovascular Surgical ProceduresSurgical Procedures, OperativeVascular GraftingVascular Surgical ProceduresThoracic Surgical ProceduresEndovascular ProceduresMinimally Invasive Surgical Procedures

Study Officials

  • Sefa SURAL, MD

    Toros University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor of Cardiology

Study Record Dates

First Submitted

January 17, 2026

First Posted

January 28, 2026

Study Start

September 10, 2025

Primary Completion

December 31, 2025

Study Completion

January 15, 2026

Last Updated

January 28, 2026

Record last verified: 2026-01

Data Sharing

IPD Sharing
Will not share

Individual participant data will not be shared due to the retrospective design of the study and institutional data privacy policies.

Locations