[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"fenestrated-endovascular-aortic-repair\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:fenestrated-endovascular-aortic-repair":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,52,83],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":22,"studyType":23,"phases":4,"briefSummary":24,"conditions":25,"keywords":32,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":41,"lastUpdatePostDateStruct":42,"startDateStruct":45,"completionDateStruct":47,"leadSponsor":49,"locationsCount":4},"100629878","real-world-data-collection-of-gore-devices-used-in-the-endovascular-treatment-of-aortic-aneurysms-which-incorporate-visceral-arteries-100629878",false,"NCT07480395","Real-World Data Collection of GORE Devices Used In the Endovascular Treatment of Aortic Aneurysms Which Incorporate Visceral Arteries.","The ENVISION Registry: REal-World Data CollectioN of GORE deVIceS Used In the endOvascular treatmeNt of Aortic Aneurysms Which Incorporate Visceral Arteries.","ENVISION","Inclusion Criteria:\n\n1. Informed Consent Form (ICF) is signed by Subject.\n2. Age ≥ 18 years at time of informed consent signature.\n3. Patient presents with thoracoabdominal, pararenal, juxtarenal, or short-neck infrarenal aortic pathology suitable for endovascular repair.\n4. Patient requires the incorporation of ≥ 1 visceral artery and is suitable for use of at least 1 GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis (BXB) as a bridging stent (Note: Up to six (6) visceral arteries may be incorporated).\n5. Patient is willing to adhere to the institutional standard of care follow-up.\n\nExclusion Criteria:\n\n1. Patient has a prior visceral artery stenting not associated with registry procedure.\n2. Patient treated for acute or sub-acute dissection, \\\u003C90 days from onset of symptoms\n3. Patient is intended to be treated with a parallel grafting (e.g., chimney, periscope, sandwich) or octopus technique.\n4. Known hypersensitivity to heparin or a previous incident of Heparin-Induced Thrombocytopenia (HIT) type II.\n5. Patient has known coagulation disorders including hypercoagulability that are not amenable to treatment.\n6. Patient has a life expectancy \\\u003C 1-year.\n7. Patient is participating in an investigational study which may confound registry results, unless approved by Gore","ALL","18 Years",{"count":20,"type":21},400,"ESTIMATED","5 Years","OBSERVATIONAL","The registry population consists of patients presenting with complex aortic pathologies amenable to endovascular aortic repair that requires the incorporation of bridging stents to maintain visceral artery perfusion",[26,27,28,29,30,31],"Complex Aortic Aneurysms","Thoracoabdominal Aneurysm","Fenestrated Endovascular Aortic Repair","Endovascular Aortic Repair","Abdominal Aorta Aneurism","Chronic Dissection",[33,34,35,36,37,38,39],"FEVAR","BEVAR","TAAA","AAA","Visceral","aortic aneurysm","PMEGs","NOT_YET_RECRUITING","2026-05-27",{"date":43,"type":44},"2026-06-01","ACTUAL",{"date":46,"type":21},"2026-12",{"date":48,"type":21},"2035-12",{"name":50,"class":51},"W.L.Gore & Associates","INDUSTRY",{"id":53,"slug":54,"hasResults":11,"nctId":55,"briefTitle":56,"officialTitle":57,"acronym":58,"eligibilityCriteria":59,"healthyVolunteers":11,"sex":17,"minAge":60,"maxAge":4,"enrollmentInfo":61,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":63,"conditions":64,"keywords":67,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":82},"100629483","svf-treo-study-influence-of-cardiac-and-respiratory-pulsatility-deformation-100629483","NCT07475260","SVF-Treo Study: Influence of Cardiac and Respiratory Pulsatility Deformation","Investigating the Influence of Cardiac and Respiratory Pulsatility Deformation on the Abdominal Aorta Before and After the Implantation of the Fenestrated TREO.","SVF-Treo","Inclusion Criteria:\n\n* Asymptomatic AAA,\n* Age \\> 65\n* Indication for AAA treatment according to standard practice\n* Anatomic suitability for the fenestrated Treo stent graft\n* At least one stentable main renal artery and one other stentable renal or mesenteric artery\n* Being able to hold their breath for 10 seconds.\n\nExclusion Criteria:\n\n* No informed consent obtained\n* eGFR \\\u003C 30 ml\u002Fmin\n* Allergy for intra venous contrast fluid.","65 Years",{"count":62,"type":21},25,"This is a national multicenter study with 25 patients with a complex AAA undergoing endovascular repair with the Fenestrated TREO™ stent graft. ECG and respiratory-gated CT scans will be performed pre-operatively, at discharge, after 6 months, and after 12 months follow up. If stent movement is still present in after 12 months, then another scan will be taken at 24 months. To include respiratory gated with the ECG-gated, patients will undergo ECG-gated CT scan during an inspiration breath-hold as well as an expiration breath-hold. This double gated CT scans will allow us to analyse the movement of the stent graft caused by the cardiac cycle and respiratory cycle.\n\nThe duration of this study is 2.5 years.",[65,66,28],"Abdominal Aortic Aneurysm","Endovascular Abdominal Aortic Aneurysm Repair",[65,68,33,69,70,71],"Endovascular Aneurysm Repair","Computed Tomography Imaging","CT","ECGgated","2026-03-16",{"date":74,"type":44},"2026-03-19",{"date":76,"type":21},"2026-04-01",{"date":78,"type":21},"2028-01-31",{"name":80,"class":81},"University of Twente","OTHER",6,{"id":84,"slug":85,"hasResults":11,"nctId":86,"briefTitle":87,"officialTitle":88,"acronym":89,"eligibilityCriteria":90,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":91,"targetDuration":4,"studyType":93,"phases":94,"briefSummary":96,"conditions":97,"keywords":98,"overallStatus":103,"whyStopped":4,"lastUpdateSubmitDate":104,"lastUpdatePostDateStruct":105,"startDateStruct":107,"completionDateStruct":109,"leadSponsor":111,"locationsCount":113},"100625611","beflared-versus-vbx-for-fevar-100625611","NCT07424885","BeFlared Versus VBX for FEVAR","BeFlared FEVAR Stent Graft System© Versus GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis for Fenestrated Endovascular Aortic Repair - Randomized Controlled Unblinded Clinical Trial","BRAVE FEVAR","Inclusion Criteria:\n\n* written informed consent form signed by the patients before admission to the study;\n* age \\> 18 years;\n* power of judgement and understanding capability of person;\n* patients with juxtarenal, pararenal, paravisceral AAA, EL Type IA with a previous history of EVAR procedure or TAAA (extent I-IV in accordance with Crawford Classification) undergoing emergency\u002Felective treatment with FEVAR (custom-made or off-the-shelf endograft) at the Division of Vascular Surgery, Department of General Surgery, Medical University of Vienna.\n\nExclusion Criteria:\n\n* age \\\u003C 18 years;\n* all female patients with a pregnancy possibility (premenopausal)",{"count":92,"type":21},126,"INTERVENTIONAL",[95],"NA","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).\n\nPrimary objectives:\n\n* compare cumulative device time between patients undergoing FEVAR with BeFlared and VBX brindging device;\n* compare target vessel (TV) instability at early, short-term and midterm follow-up in patients undergoing FEVAR with BeFlared and VBX brindging device.\n\nSecondary objectives:\n\n\\- compare intraoperative TV technical success in patients undergoing FEVAR with BeFlared and VBX bridging device.",[28],[33,99,100,101,102],"endovascular aortic repair","bridging stent graft","cannulation","target vessel instability","RECRUITING","2026-02-24",{"date":106,"type":44},"2026-02-27",{"date":108,"type":44},"2026-02-19",{"date":110,"type":21},"2033-02",{"name":112,"class":81},"Medical University of Vienna",1]