Heart Disease Trial, Recruiting NCT06002932 Sponsor: Saint Vincent's Hospital, Korea Condition: Heart Disease
Back to Heart Disease

Heart Disease Trial, Recruiting

NCT06002932
Recruiting Not Applicable

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 16 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

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

Status
Recruiting
Phase
Not Applicable
Sponsor
Saint Vincent's Hospital, Korea
Registry
ClinicalTrials.gov
Start date
8 September 2023
Est. completion
31 July 2028

Where this trial is recruiting

🇰🇷 South Korea

Primary endpoints

target lesion failure the number of events

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

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.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov