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NCT03190057: IRISBioFreedom
IRIS-BioFreedom Cohort in the IRIS-DES Registry
trial testing BIOFREEDOM™ FAMILY stent in Coronary Stenosis in 218 participants. Terminated before completion.
29 September 2025
Quick facts
| Lead sponsor | Seung-Jung Park |
|---|---|
| Status | Terminated |
| Study type | OBSERVATIONAL |
| Enrollment | 218 |
| Start date | 20 May 2019 |
| Primary completion | 29 September 2025 |
| Estimated completion | 29 September 2025 |
| Sites | 8 locations across South Korea |
Drugs / interventions tested
- BIOFREEDOM™ FAMILY stent
Conditions studied
- Coronary Stenosis — all drugs for Coronary Stenosis →
Sponsor
Seung-Jung Park — full company profile →
Who can join
19 and older, any sex, with Coronary Stenosis. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
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.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT03190057
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Coronary Stenosis
Currently open trials in the same condition.
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- NCT05709652 — Impact of Fast-rotation Coronary CT in Patients Undergoing Aortic Stenosis Workup · NA · recruiting
- NCT06376630 — Study of Microvascular Dysfunction, CFR and Cardioprotective Effect of Early Administration of Esmolol in MI · NA · recruiting
- NCT04014140 — iFR Guided Coronary Artery Bypass Grafting Surgery · recruiting
Other Seung-Jung Park trials
Trials by the same sponsor.
- NCT06908499 — The DECISION-CTO Extended 10 Y Follow-up · not yet recruiting
- NCT06177743 — IRIS-Coroflex NEO Cohort · recruiting
- NCT05125367 — Ten-Year Outcomes of Randomized Comparison of Coronary Artery Bypass Surgery and Everolimus-Eluting Stent Implantation i · completed
- NCT03967158 — Evaluation of Effectiveness and Safety of XIENCE Sierra in Routine Clinical Practice · active not recruiting
- NCT03871127 — Ten-Year Outcomes of PRE-COMBAT Trial · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT03190057 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Seung-Jung Park
- Last refreshed: 30 September 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03190057.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing