Condition: Acute Coronary Syndrome · Sponsor: Yonsei University
To test whether the polymer-free drug-coated stent (DCS) BioFreedom is noninferior to the biodegradable polymer drug-eluting stent (DES) Ultimaster in terms of 1-year patient-oriented composite endpoint (POCE, composite of all-cause mortality, any MI, or any revascularization) in a setting of 1-month dual-antiplatelet therapy (DAPT) strategy (1-month DAPT followed ticagrelor monotherapy) after acute coronary syndrome.
This description comes directly from the study's public registry record.
Chul-Min Ahn · +82-2-2228-8532 · drcello@yuhs.ac
Sung-Jin Hong, MD, PhD · +82-2-2228-8452 · hongs@yuhs.ac
Always discuss trial participation with your own doctor first.
| Yonsei Cardiovascular Hospital, Yonsei University College of Medicine | Seoul, South Korea | Recruiting |
Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.
We email about this public record only. Unsubscribe anytime with one click. Never medical advice.
This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.
Source record: clinicaltrials.gov/study/NCT05305482