Condition: Fenestrated Endovascular Aortic Repair · Sponsor: Medical University of Vienna
This randomized controlled unblinded trial aimes to compare BeFlared FEVAR Stent Graft System (BeFlared) with GORE® VIABAHN® VBX Balloon Expandable Endoprothesis (VBX) in patients undergoing endovascular aneurysm repair with fenestrated device (FEVAR). Primary objectives: * compare cumulative device time between patients undergoing FEVAR with BeFlared and VBX brindging device; * compare target vessel (TV) instability at early, short-term and midterm follow-up in patients undergoing FEVAR with BeFlared and VBX brindging device. Secondary objectives: \- compare intraoperative TV technical success in patients undergoing FEVAR with BeFlared and VBX bridging device.
This description comes directly from the study's public registry record.
Wolf Hans Eilenberg, MD, PhD · +43 (0)1 40400-69560 · wolf.eilenberg@meduniwien.ac.at
Anna Sotir, MD · anna.sotir@meduniwien.ac.at
Always discuss trial participation with your own doctor first.
| Medical University of Vienna, Department of General Surgery, Division of Vascular Surgery | Vienna, State of Vienna, Austria | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07424885