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Across meta-analyses, head-to-head RCTs and real-world studies, Eluvia's outcomes hold up study after study. As new data is released, you'll find it here: another study, another reason Eluvia is THE STANDARD.
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TCT | VEITH | PVI
ELEGANCE Registry 12 Month Data Set1
Released Oct 6th, 2026
- ELEGANCE Registry Page 1
- ELEGANCE Registry Page 2
- ELEGANCE Registry Page 3
- ELEGANCE Registry Page 4
TRUE-PTX Eluvia Subgroup Analysis2
Before matching
12-month amputations occurred less frequently for patients treated with Eluvia DES
| Eluvia | non-DE | P-value | |
|---|---|---|---|
| Any Limb Amputation | 7.7% | 8.9% | 0.265 |
| Same Limb Amputation | 1.9% | 2.3% | 0.391 |
| Any Readmission | 51.9% | 57.8% | 0.001 |
After Matching3
Patients treated with non-DE devices were more likely to have any above-ankle amputation and any readmission compared with Eluvia DES
Treatment with a non-DE device increased odds for any above-ankle amputation by
47%
Treatment with a non-DE device increased odds for any readmission by
23%
References:
1. Secemsky E, on behalf of the ELEGANCE Investigators. 12-month Outcomes for Patients with Complex PAD Treated with Eluvia DES from the ELEGANCE Registry. VIVA 2026 Scientific Sessions, Las Vegas, NV; 2026.
2. Brian DeRubertis. Polymer-based Drug-Eluting Stent vs Bare Device Therapies for PAD In the Real World: 12-Month Amputation and Readmission Rates in a Large Nationwide Population. Presented at CX 23 April 2025.
3. Exact Matching Method.