The UltimasterTM Clinical
Program included more than 50,000 patients covering 16 CE marked indications.
Demonstrates favourable outcomes in both complex and non-complex PCI patients.
Demonstrates Proximal Optimisation Technique is associated with improved outcomes.
Suggests that complete revascularisation is associated with better outcomes versus incomplete revascularisation.
The UltimasterTM Clinical Program included one of the largest, prospective worldwide registries, the e- ULTIMASTER™ with 37,198 patients. The Ultimaster™ Clinical Program² demonstrates the safe and effective use of the Ultimaster stent in different patient cohorts, representative of daily PCI practice.
Largest study to date on 1-year outcomes post-PCI, in an unselected, real-world cohort of patients enrolled in the e-ULTIMASTER registry.The aim of the study was to understand the prevalence, clinical characteristics, and 1-year outcomes of patients with complex lesions in an unselected cohort of over 35,000 patients who underwent PCI with the Ultimaster™ DES system.”
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Discover our clinical evidence and case studies concerning this topic.
Featured product: Ultimaster™ Sirolimus Eluting Coronary Stent System
Featured products: Ultimaster™ Sirolimus Eluting Coronary Stent System, Ultimaster™ Tansei™ Sirolimus Eluting Coronary Stent System
500 STEMI patients, randomised 1:3 vs Kaname BMS, primary endpoint TVF 12M. Published and completed
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