Safety and efficacy of a bioresorbable vascular scaffold for the side branch in coronary bifurcation lesions: A clinical feasibility trial
Not Applicable
- Conditions
- Coronary artery disease with bifurcation lesions
- Registration Number
- JPRN-UMIN000016726
- Lead Sponsor
- Public interest incorporated foundation Ohara HealthCare Foundation Kurashiki Central Hospital Department of Cardiology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
(1)Unable to be followed up by the implementing medical institution (2)Life expectancy <2 years (3)Allergic or contraindicative to the materials used for BVS (4)Scheduled for elective treatment requiring antiplatelet drug withdrawal (5)Possibility of pregnancy or lactation (6)Deemed as unsuitable by the investigator or sub-investigator
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The late loss of the side branch in bifurcation at 8 and 20 months after PCI.
- Secondary Outcome Measures
Name Time Method