Read the analysis of the ENCHANT trial, which assesses the clinical outcomes, safety, and performance of the Endurant II/IIs system used with balloon-expandable covered stents.
Proven device combination for ChEVAR
EnChEVAR with Endurant™ II/IIs system + Radiant™ covered stent demonstrates durable clinical outcomes (mean f/u 24.6 ± 17.4 months)1:
Proven, safe, and effective way to lengthen aortic sealing zones
Learn how EnChEVAR with Endurant™ II/IIs system + Radiant™ stent provides durable outcomes in challenging hostile sealing zones.
EnChEVAR deployment
Step-by-step deployment of the EndurantT™II/IIs and Radiant™ stent grafts for ChEVAR.||
EnChEVAR live case
Explore a unique real live case performed by Prof. Fazzini in a 3 min video.
EnChEVAR (Endurant II/IIs stent graft system + Radiant† balloon-expandable covered stent) analysis (n = 62)3
ENCHANT is a multicentre, prospective, single-arm, post-market study to assess the clinical outcomes, safety, and performance of the Endurant II/IIs system used with balloon-expandable covered stents for treatment of juxtarenal aortic aneurysms with a short infrarenal neck in a real-world setting.
One year sac status by Core Lab (n = 41)‡
The PROTAGORAS study1 evaluated the performance of the Endurant™ II/IIs stent graft for patients with pararenal pathologic processes that were treated by the chemistry/snorkel endovascular technique.
Standardised use of the Endurant™ II/IIs stent graft system and Radiant™ covered stent for ChEVAR demonstrated:
Radiant™ covered stent shows significantly better performance in ChEVAR compared to other grafts, with 94.6% patency at midterm compared to 84.1% patency with other covered stents.2
View brochure for full details.
Dr. Fazzini explains the benefits of the combination of Endurant™ II/IIs system and Radiant™ stent: safer procedure, shorter recovery times, and lower of reintervention rate.
Prof. Reijnen and Prof. Donas share their clinical experience about EnChEVAR technique with Endurant™ II/IIs system and Radiant™ covered stent.
Vessel proximal diameter: |
Vessel proximal diameter: infrarenal ChEVAR (mm) |
Proximal stent graft diameter (mm) |
|---|---|---|
| 19–20 | N/A | 23 |
| 21–22 | 19–20 | 25 |
| 23-25 | 21–23 | 28 |
| 26-28 | 24–26 | 32 |
| 29–32 | 27–30 | 36 |
Renal native diameter (mm) |
Recommended Radiant diameter (mm) |
|---|---|
| 5.4–6.2 | 6 |
| 6.3–7.2 | 7 |
Diameter (mm) |
Stent length (mm) |
Catheter length (cm) |
Catheter outer diameter (Fr) |
|---|---|---|---|
| 6 | 22 | 120 | 6 |
| 6 | 32 | 120 | 7 |
| 6 | 38 | 120 | 7 |
| 6 | 59 | 120 | 7 |
| 7 | 22 | 120 | 7 |
| 7 | 32 | 120 | 7 |
| 7 | 38 | 120 | 7 |
| 7 | 59 | 120 | 7 |
Use this tool to see full ordering information and plan case specifics such as sizing and placement.
Shorter 16 F sheath or larger may be used for access during a two-chimney case.
Must be able to pass through and extend beyond 90 cm sheath; variety of angles to support renal cannulation; vertebral multipurpose.
Brief statement: See the device manual for detailed information regarding the instructions for use, the implant procedure, indications, contraindications, warnings, precautions, and potential adverse events. For further information, contact your local Medtronic representative and/or consult the Medtronic website at medtronic.eu. For applicable products, consult instructions for use on www.medtronic.com/manuals. Manuals can be viewed using a current version of any major internet browser. For best results, use Adobe Acrobat® Reader with the browser.
™ Third-party brands are trademarks of their respective owners.
† Patients in this dataset were treated with Advanta V12, which was re-labelled as Radiant and received CE mark approval in September 2022 for use in ChEVAR.
‡ Denominator is the number of subjects with Core Lab-reported maximum aneurysm diameter at both one month post-implant and one-year follow-up.
§ Other covered stents include: GORE Viabahn®*, Bentley BeGraft™*, BD LifeStream™*.
|| All indications related to the EndurantTM II/IIs and RadiantTM stent grafts are not approved globally. Please check your local regulatory approval status. Refer to the complete Instructions for Use manual of the EndurantTM II/IIs and RadiantTM stent grafts for the indications approved in your geography.
1. Donas KP, Torsello GB, Piccoli G, et al. The PROTAGORAS study to evaluate the performance of the Endurant stent graft for patients with pararenal pathologic processes treated by the chimney/snorkel endovascular technique. J Vasc Surg. January 2016;63(1):1–7.
2. Pitoulias GA, Torsello G, Austermann M, et al. Outcomes of elective use of the chimney endovascular technique in pararenal aortic pathologic processes. J Vasc Surg. February 2021;73(2):433–442.
3. Prof. Giovanni Torsello. "ENCHANT Trial interim analysis: Endurant ChEVAR technique for juxtarenal aneursyms. "Presented at LINC, June 8, 2023; Leipzig, DE.
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