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JDEPTH-LM Registry

JDEPTH-LM Registry: Japanese Coronary Intervention using Drug Eluting and Perfusion Therapy for Left Main Disease

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-jRCT1030240071
Enrollment
280
Registered
2024-05-09
Start date
2024-05-27
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stable angina, non-ST-elevation acute coronary syndrome, Unstable angina Ischemic heart disease

Interventions

None listed

Sponsors

Warisawa Takayuki
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Age >= 18 years 2. Patient with stable coronary artery disease, non-ST-elevation myocardial infarction, or unstable angina 3. Left main disease confirmed by coronary angiography or coronary CT angiography 4. Clinical and anatomical eligibility for PCI as agreed by the local Heart Team 5. Patient with consent prior to undergoing PCI 6. Left main Medina classification (1,1,1), (1,0,1), (0,1,1) and (0,0,1) confirmed by coronary angiography 7. De novo target lesion in LMT-LAD amenable for crossover stenting with provisional side-branch approach as determined by PCI operator 8. De novo ostial LCx lesions 9. Lesion indicated in No. 8 with a length of less than 10 mm or a stenosis of less than 70% confirmed by coronary angiography

Exclusion criteria

Exclusion criteria: 1. Inability to provide written informed consent 2. Patient with a history of ST-elevation myocardial infarction within the previous 1 week 3. Patient in a state of cardiogenic shock 4. Patient with a history of coronary artery bypass grafting 5. Patient with malignant tumors or other conditions with a life expectancy of less than one year 6. Patient considered suitable for stent placement in the ostial LCx from a medical perspective 7. Patient considered unsuitable for anti-thrombotic therapy after PCI 8. Other patient whom the investigator deems unsuitable for the safe conduct of LM-PCI, including W-KBT

Design outcomes

Primary

MeasureTime frame
1. Procedure success rate: indicating the proportion of cases meeting the following three conditions: - Device delivery success - Achievement of DCB expansion for 30 seconds or more - No bailout stenting performed in the LCx 2. MACE at 12 months: consisting of all-cause mortality, nonfatal MI, and ischemia-driven unplanned revascularization for left main disease

Secondary

MeasureTime frame
- Time to ST-change from DCB inflation - Total DCB Inflation time - Maximum changes in blood pressure and heart rate - Use of vasopressors, inotropes, and mechanical circulatory support systems after W-KBT - Incidence cases for each component of MACE and ischemia-driven unplanned revascularization for lesions at the LCx ostium

Contacts

Public ContactShuhei Odagiri

TCROSS Co., Ltd.

s-odagiri@tcross.co.jp+81-3-5341-4670

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026