Trials / Terminated
TerminatedNCT03190057
IRIS-BioFreedom Cohort in the IRIS-DES Registry
Evaluation of Effectiveness and Safety of BIOFREEDOM™ FAMILY Stent in Routine Clinical Practice; A Multicenter, Prospective Observational Study
- Status
- Terminated
- Phase
- —
- Study type
- Observational
- Enrollment
- 218 (actual)
- Sponsor
- Seung-Jung Park · Academic / Other
- Sex
- All
- Age
- 19 Years
- Healthy volunteers
- Not accepted
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.
Detailed description
BIOFREEDOM™ FAMILY stent means that Biofreedom stent, Biofreedom Ultra and the other stents with names starting with Biofreedom.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | BIOFREEDOM™ FAMILY stent | Percutaneous coronary intervention with BIOFREEDOM™ FAMILY stent |
Timeline
- Start date
- 2019-05-20
- Primary completion
- 2025-09-29
- Completion
- 2025-09-29
- First posted
- 2017-06-16
- Last updated
- 2025-09-30
Locations
8 sites across 1 country: South Korea
Source: ClinicalTrials.gov record NCT03190057. Inclusion in this directory is not an endorsement.