IRIS-BioFreedom Cohort in the IRIS-DES Registry

NCT03190057 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 218

Last updated 2025-09-30

No results posted yet for this study

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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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03190057 on ClinicalTrials.gov