JPRN-jRCTs052200077Recruiting未知
Comparison of Drug-Coated versus Conventional Balloonsfor the Side Branch of the Bifurcation Lesion- MULTICENTER RANDOMIZED CONTROLLED STUDY
Sakata Yasushi0 sites300 target enrollmentStarted: October 28, 2020Last updated:
Conditions
Trial Snapshot
- Phase
- 未知
- Status
- Recruiting
- Sponsor
- Enrollment
- 300
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- >= 20age old to ot applicable (—)
- Sex
- All
Inclusion Criteria
- •Patients who satisfy all of the following inclusion criteria and none of the exclusion criteria are enrolled in the present study.
- •1. Patients aged at least 20 years at the time of their consent
- •2. Patients who agree to be enrolled in the study giving signed written informed consent
- •3. Patients undergoing a first-time PCI in bifurcation
- •4. Patients undergoing PCI in bifurcation with a side branch 2.0-3.0 mm in diameter
- •5. Patients undergoing PCI in bifurcation which is intended to be treated with a single stenting strategy (DES implantation in only main branch)
- •6. Patients who can receive dual antiplatelet therapy according to the latest guideline
- •7. Patients who agree to receive coronary angiography 9 months after PCI
Exclusion Criteria
- •Patients are excluded from this study if they have the following criteria.
- •1. Patients who are pregnant or breast-feeding
- •2. In-stent restenosis
- •3. Lesion in the bypass graft
- •4. Lesion with acute coronary syndrome
- •5. Patients who developed acute myocardial infarction within 1 month
- •6. Patients complicated with active bleeding
- •7. Patients who are participating in intervention study, or who are participating or are scheduled to participate in clinical trial or clinical study with intervention before the end of the follow-up of the present study
- •8. Life expectancy within 1 year
- •9. Hemodialysis
- •10. Lesion with total occlusion
- •11. Patients who are judged as inappropriate subjects for the present study by the principal investigator or collaborators
Investigators
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