The Supera™ Stent has been studied in over 2,000 patients worldwide in the SUPERB trial and 16 retrospective studies. Notably, in all of the 17 studies, the Supera™ Peripheral Stent showed durable results with zero fractures at 1 year.1,4-19
At 1 year the Supera™ Stent demonstrated primary patency of 91% when nominally* deployed. At 3 years, freedom from targeted lesion revascularisation (TLR) was 94% when nominally* deployed.1
PATENCY (K-M) AT 1 YEAR
When nominally deployed*
FREEDOM FROM TLR AT 3 YEARS
When nominally deployed*
*Nominal deployment is defined as the stent length upon deployment being within +/- 10% of the labelled stent length. This data is from a non-powered post-hoc analysis. K-M=Kaplan Meier.
With some peripheral stents, increasing lesion lengths can lead to decreasing patency rates.20 The Supera™ Stent stands apart for its consistently high patency rates in lesions spanning lengths from 5.3 cm up to 28.0 cm.†
† Published data was included if lesion length and patency were both available.
Note: Results from different clinical trials are not directly comparable. Information provided for educational purposes only.
Whether treating simple (TASC A&B) or complex (TASC C&D) lesions, the Supera™ Stent is associated with impressive, consistent patency performance data at 1 year.1-4
Simple | |||
---|---|---|---|
Trial/Study | MUNICH REGISTRY2 | SUPERB1 | |
Lesion Length | 5.3cm | 7.8cm | |
TASC A&B Lesions | 100% | 94% | |
1-Yr Patency | 86.7% | 90.5% | |
Sites | Single Centre | Multicentre (46 sites) | |
# Patients | 70 | 264 |
Complex | |||
---|---|---|---|
Trial/Study | ST. LOUIS4 | SUPERSUB3 | |
Lesion Length | 24cm | 28cm | |
TASC C&D Lesions | 78% | 100% | |
CTOs | Unknown | 100% | |
1-Yr Patency | 85.6% | 94.1% | |
Sites | Single Centre | Single Centre | |
# Patients | 48 | 34 |
TASC: Trans-Atlantic Inter-Society Consensus
MAT-2409315 v1.0
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MAT-2105201 v1.0