A study in people with coronary artery stenosis.

Recruiting now. Registry record last updated June 24, 2026.

Who can join
Adults 20+, have coronary artery stenosis.
What you take
Check ClinicalTrials.gov for this trial's study groups and what each group receives.
How long it lasts
The full study runs about 6 years.
What you get
Costs vary by study. Ask the study team what this one covers, including the study medicine, visits and travel, before you sign the consent form.
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Phase Not ApplicableSponsor Duk-Woo Park, MDDrug investigational drugClass OtherSites 1 USEnrollment target 1,500

What this study is for

Primary condition: Coronary Artery Stenosis.

Full scientific study title: Diabetes-Centered Evaluation of Revascularization Strategy of Functional and Imaging-CombiNEd State-of-the-Art Percutaneous Coronary Interve.

Who can join

Age20 and upSexAny

Adults 20+, have coronary artery stenosis. A site coordinator confirms whether you qualify during a free screening visit. The exact medical requirements are below.

Full medical eligibility (for you and your doctor)verbatim from the registry

This is the exact wording from ClinicalTrials.gov, including clinical measures (lab values, imaging scores). Bring it to your doctor if any of it is unclear.

Key inclusion criteria

  • The subject must be ≥20 years of age with angina and/or evidence of myocardial ischemia.
  • Patients with type 2 diabetes based on the need for treatment with insulin or oral hypoglycemic drugs or a confirmed elevated blood glucose level (fasting plasma glucose elevation on \>1 occasion of ≥126 mg/dL \[7.0 mmol/L\] or 2-h postprandial of ≥200 mg/dL \[11.1 mmol/L\] during oral glucose tolerance test or random plasma glucose of ≥200 mg/dL \[11.1 mmol/L\] with classic symptoms of hyperglycemia or hyperglycemic crisis or HbA1C ≥6.5% \[48 mmol/mol\]).
  • Significant three-vessel CAD (defined as ≥ 50% diameter stenosis \[DS\] by visual estimation in each of the three major epicardial vessels or major side branches but not involving the left main coronary artery) and equivalently amenable to revascularization by means of either PCI or CABG as determined by the Heart Team at the trial site.
  • The patient or guardian agrees to the study protocol and the schedule of clinical follow-up, and provides informed, written consent, as approved by the appropriate Institutional Review Board/Ethical Committee of the respective clinical site.

Key exclusion criteria

  • Unprotected left main coronary artery disease.
  • The presence of complex coronary disease anatomy or lesion characteristics or other cardiac condition(s) which leads the participating interventional cardiologist to believe that PCI is not suitable (i.e. the subject should be managed with CABG or medical therapy alone).
  • Recent ST-elevation myocardial infarction(\<5 days prior to randomization).
  • Cardiogenic shock and/or need for mechanical/pharmacologic hemodynamic support.
  • Severe left ventricular dysfunction (ejection fraction \<30%).

Where this trial is enrolling

This trial has 1 sites across 1 state. Contact a site coordinator directly to start screening.

California1 site
  • Palo Alto VA Medical Center
    Palo Alto, California
    Fearon F. William, MD

Timeline

Started enrolling: June 14, 2024. Expected completion: December 31, 2029. Last updated on ClinicalTrials.gov: June 24, 2026.

Official source

Every Monday we check this trial against ClinicalTrials.gov, the federal registry for clinical research. Last checked September 4, 2026. Confirm the current status there before you contact a site:

View on ClinicalTrials.gov →

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