IRIS-BioFreedom Cohort in the IRIS-DES Registry
NCT03190057 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 218
Last updated 2025-09-30
Summary
The objective of this study is to evaluate effectiveness and safety of BIOFREEDOM™ FAMILY stent in the "real world" daily practice as compared with other drug-eluting stents.
Conditions
- Coronary Stenosis
Interventions
- DEVICE
-
BIOFREEDOM™ FAMILY stent
Percutaneous coronary intervention with BIOFREEDOM™ FAMILY stent
Sponsors & Collaborators
-
CardioVascular Research Foundation, Korea
collaborator OTHER -
Seung-Jung Park
lead OTHER
Eligibility
- Min Age
- 19 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2019-05-20
- Primary Completion
- 2025-09-29
- Completion
- 2025-09-29
Countries
- South Korea
Study Locations
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