Hear IMPERIAL Principal Investigator, William Gray, MD share his perspectives on what the data means for diabetic patients.
This subgroup analysis provides clinical data on the safety and effectiveness of the Boston Scientific Corporation ELUVIA™ Drug-Eluting Vascular Stent System for treating Superficial Femoral Artery (SFA) and/or Proximal Popliteal Artery (PPA) lesions in the Diabetic patient population.
Diabetic Subgroup Baseline Characteristics
12-Month Primary Patency Results†
Eluvia demonstrated 87.4% primary patency versus 80.2% for Zilver PTX in the IMPERIAL Diabetic Subgroup.
12-Month Safety Results
Eluvia demonstrated a statistically significant reduction in TLR of greater than 70% in diabetic patients.
Eluvia demonstrated a 9-fold, statistically significant lower stent thrombosis rate in diabetic patients.
Eluvia has demonstrated remarkable and consistent primary patency
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