The objective of the study is to collect real-world data on patient outcomes and evaluate the safety and performance of the Lifetech Ankuraâ„¢ AAA Stent Graft System, Ankuraâ„¢ Cuff Stent Graft System, Ankuraâ„¢ AUI Stent Graft System and ZoeTrackâ„¢ Super Stiff Guidewire.
Who can participate
Age range18 Years – 85 Years
SexALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion criteria
✓. Patient diagnosed with Abdominal Aortic Aneurysm (AAA), who needs endovascular aortic repair;
✓. Patient's anatomy suits Ankura™ AAA and Cuff Stent Graft Systems, or AUI Stent Graft IFU requirements, which indicated by the following:
✓. Adequate iliac/femoral access vessel that is compatible with the required delivery system.
✓. Non-aneurysmal proximal aortic neck diameter of 18-32mm.
✓. Proximal aortic neck angulation ≤ 60°.
✓. Distal iliac artery anchorage zone ≥15mm.
✓. Distal iliac artery diameter of i. 8-22 mm (for Ankura™ AAA and Cuff Stent Graft Systems), OR ii. 10-16 mm (for Ankura™ AUI Stent Graft System).
Exclusion criteria
✕. Age\<18 years or Age\>85 years;
✕. Patients' life expectancy \< 1 year;
✕. Pregnant or plan to be pregnant or breast feeding;
✕. Patient with any contraindications mentioned in the Ankura™ AAA and Cuff Stent Graft Systems, or in Ankura™ AUI Stent Graft system IFU: