Heart Disease Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People aged 19 years or older.
- People who have a specific type of blocked artery at a branching point in the heart, where the branch vessel measures between 2.25 and 2.75 mm wide, the main vessel is at least 2.5 mm wide, and the blockage meets a specific pattern called a "true bifurcation" (Medina classification 1,1,1), (1,0,1), or (0,1,1) — this is a new blockage, not a previously treated one (confirm with trial site).
- People whose heart condition is diagnosed as stable chest pain (stable angina), unstable chest pain (unstable angina), or a certain type of heart attack (non-ST elevation myocardial infarction), at least 24 hours after their last treatment for that condition.
- People who have been fully informed about the trial, understand the risks involved, and have given their written consent to participate — either personally or through a legal representative.
Who may not be able to join:
- People who have had a specific type of serious heart attack (ST-elevation myocardial infarction), or who have a true bifurcation blockage in the left main coronary artery.
- People whose treating doctor has decided that a two-stent procedure is not appropriate for their condition.
- People who cannot take aspirin or certain blood-thinning medications called P2Y12 inhibitors (such as ticagrelor or clopidogrel) due to a medical contraindication.
- People who experienced severe circulatory collapse (cardiogenic shock) at hospital admission, or who have significantly reduced heart pumping function (left ventricle ejection fraction below 30%).
- People who need to take long-term blood-thinning medication, such as warfarin or a newer oral anticoagulant (NOAC).
- People who are currently bleeding, or who are considered at high risk of serious bleeding (for example, due to active stomach ulcers, certain digestive tract conditions, or tumours with a high bleeding risk).
- People with a history of bleeding in the brain or a brain aneurysm.
- People who have a surgical procedure planned within the next six months that would require stopping blood-thinning medication.
- People with severe liver disease (including fluid build-up in the abdomen), a very low platelet count (below 80,000 cells/mm³), or a low haemoglobin level (below 10 g/dL).
- People considered at risk of an abnormally slow heart rate, including those with a significant heart rhythm conduction problem (grade 2 or higher atrioventricular block) who do not have a permanent pacemaker.
- People who are pregnant (based on a positive pregnancy test) or currently breastfeeding.
- People whose doctor estimates they have less than one year of life expectancy due to other serious health conditions.
- People who are already taking part in another clinical trial for a different medicine or medical device, where the main study results have not yet been collected.
- People who have not signed an informed consent form, or who cannot be reliably followed up over the long term.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Sung-Ho Her, MD. PhD., St Vincent's Hospital
Phone: +82312598397
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
target lesion failure the number of events
Can't join this trial?
Data last synced from ClinicalTrials.gov: 16 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.