WebOct 12, 2015 · Patients were randomized to either Biofreedom DCS (n = 1,221) or Gazelle BMS (n = 1,211). Total number of enrollees: 2,432; Duration of follow-up: 2 years; Mean patient age: 75.7 years ... The results of this trial indicate that clinical outcomes following biolimus A9 DCS implantation are superior to BMS in patients with high bleeding risk and ... WebMethods: The BioFreedom US IDE feasibility trial was a single-arm, open-label, prospective study of patients requiring stenting of de novo lesions. Patients received 3 months of DAPT, repeat angiography at 9 months, and clinical follow-up at multiple intervals. A subgroup also underwent intravascular ultrasound (IVUS) interrogation.
Leaders Free III: BioFreedom Clinical Trial - CenterWatch
WebJun 25, 2024 · Aims: The aim of this study was to evaluate the efficacy of the new BioFreedom Ultra drug-coated stent with a thin-strut cobalt-chromium platform (BF-CoCr) compared to the BF-SS in an all-comers population undergoing percutaneous coronary intervention (PCI). Methods: This was a prospective, multicentre, non-inferiority trial. WebOct 14, 2015 · stent, the BioFreedom stent (Biosensors Europe), has been developed that transfers umirolimus (also known as biolimus A9), a highly lipophilic ... the trial protocol by Centre Européen de Recher - ray rumsby
BIOSENSORS ANNOUNCES PRIMARY ENDPOINT DATA RELEASE …
WebBioFreedom™ DCS LEADERS FREE 1 was the first clinical trial to evaluate a one-month ultra-short course of DAPT in High Bleeding Risk (HBR) patients with mixed comorbidities. Superior safety and efficacy over the previous gold standard treatment was demonstrated. WebApr 9, 2024 · Detailed Description. Prospective, multi-center, open-label single-arm study designed to enroll 370 HBR patients (for at least 340 evaluable) at up to 20 centers in up to 2 European countries. 370 patients will receive a BioFreedomTM CoCr stent. All patients will be followed up for 2 years. WebNov 15, 2024 · The One-Month DAPT trial showed that 1 month of DAPT was noninferior to 6-12 months of DAPT at preventing adverse ischemic/bleeding events. ... In the 1-month DAPT group, patients received a polymer-free drug-coated stent (BioFreedom). In the 6- to 12-month DAPT group, patients received a contemporary drug-eluting stent (Biomatrix or … ray ruiz singer