[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"juxtarenal-abdominal-aortic-aneurysm\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:juxtarenal-abdominal-aortic-aneurysm":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,46],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":27,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100597997","university-of-utah-ps-ide-physician-modified-endovascular-grafts-for-the-treatment-of-elective-symptomatic-or-ruptured-juxtarenal-aortic-aneurysms-100597997",false,"NCT07065760","University of Utah PS-IDE: Physician Modified Endovascular Grafts for the Treatment of Elective, Symptomatic or Ruptured Juxtarenal Aortic Aneurysms","Physician Modified Endovascular Grafts for the Treatment of Elective, Symptomatic or Ruptured Juxtarenal Aortic Aneurysms","Inclusion Criteria:\n\n1. Patient is ≥ 18 years of age\n2. Patients who are male or non-pregnant female (females of child bearing potential must have a negative pregnancy test prior to enrollment into the study)\n3. Patient or Legally Authorized Representative has signed an Institutional Review Board (IRB) approved Informed Consent Form\n4. Patient has a juxtarenal abdominal aortic aneurysm that meets at least one of the following:\n\n   1. An aneurysm with a maximum diameter of ≥ 5.5 cm for male (≥ 5.0 cm for female) or 2 times the normal diameter just proximal to the aneurysm using orthogonal (i.e., perpendicular to the centerline) measurements\n   2. Aneurysm with a history of growth \\> 0.5 cm in 6 months\n   3. Saccular aneurysm deemed at significant risk for rupture\n   4. Symptomatic aneurysm\n   5. Ruptured aneurysm\n5. Patient has patent iliac or femoral arteries, with or without the use of conduit, that will allow endovascular access with the physician modified endovascular graft.\n6. Patient has a suitable non-aneurysmal proximal aortic neck of ≥ 2 mm inferior to the most distal renal artery ostium.\n7. Patient has a suitable non-aneurysmal distal iliac artery length (seal zone) of ≥ 15mm. The resultant repair should preserve patency in at least one hypogastric artery.\n8. Patient has a suitable non-aneurysmal proximal aortic neck diameter between 20 and 32 mm, averaged across the diameters at the Celiac, SMA, at the lowest patent renal artery and at the midpoint of the renal arteries.\n9. Patient has suitable non-aneurysmal distal common iliac diameters between 8 and 20 mm.\n10. Patient has juxtarenal aortic neck angulation ≤ 60°\n11. Target branch vessel diameter ≥ 5 mm.\n12. Patient must be willing to comply with all required follow-up exams.\n\nExclusion Criteria:\n\n1. Patient has a mycotic aneurysm or has an active systemic or local infection that may increase the risk of endovascular infection\n2. Patient has unstable angina (defined as angina with a progressive increase in symptoms, new onset at rest or nocturnal angina, or onset of prolonged angina)\n3. Patient has a major surgical or interventional procedure, not related to the endovascular repair, planned within +\u002F- 30 days of the AAA repair.\n4. Patient has history of an aortopathic connective tissue disease (e.g. Marfan's or Ehler's-Danlos syndrome).\n5. Patient has a known hypersensitivity or contraindication to anticoagulation or contrast media that is not amenable to pre-treatment.\n6. Patient has known allergy or intolerance to stainless steel, nitinol or gold (gold-coated tungsten).\n7. Patient has a body habitus that would inhibit X-ray visualization of the aorta\n8. Patient has a limited life expectancy of less than 1 year\n9. Patient is currently participating in another investigational device or drug clinical trial\n10. Patient has other medical, social or psychological conditions that, in the opinion of the investigator, preclude them from receiving the pre-treatment, required treatment, and post-treatment procedures and evaluations.\n11. Thrombus or excessive calcification within the neck of the aneurysm\n12. Branch vessel stenosis ≥ 80%\n13. Patient treatable on label with FDA approved EVAR or FEVAR device and can wait for device availability.\n14. Subject is willing and eligible to enroll in a manufacturer-sponsored study at the investigational site, or the subject is willing and eligible to participate in a study with a manufacturer-made device at another institution.","ALL","18 Years",{"count":19,"type":20},15,"ESTIMATED","INTERVENTIONAL",[23],"NA","The purpose of this study is to assess the effects of a physician-modified endovascular graft (PMEG) for juxtarenal aortic aneurysms by collecting data on its performance. Participants in the study will undergo surgery to repair their juxtarenal aortic aneurysm using the PMEG device. After the surgery, participants will attend several follow-up visits to monitor their recovery and the device's effectiveness. These follow-up visits will take place at hospital discharge, then at 1 month, 6 months, 12 months, and once a year for up to 5 years after surgery.",[26],"Juxtarenal Abdominal Aortic Aneurysm",[28,29,30,31,32],"physician modified endovascular graft","juxtarenal abdominal aortic aneurysm","PMEG","FEVAR","Endovascular Aortic Repair","RECRUITING","2026-05-13",{"date":36,"type":37},"2026-05-15","ACTUAL",{"date":39,"type":37},"2025-05-15",{"date":41,"type":20},"2032-08-01",{"name":43,"class":44},"Cali Johnson","OTHER",1,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":4,"eligibilityCriteria":52,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":53,"targetDuration":4,"studyType":21,"phases":55,"briefSummary":56,"conditions":57,"keywords":62,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":77,"lastUpdatePostDateStruct":78,"startDateStruct":80,"completionDateStruct":82,"leadSponsor":84,"locationsCount":45},"100590616","evaluation-of-clinical-efficacy-and-safety-of-aortal-stent-graft-created-using-3d-printing-technology-100590616","NCT06969729","Evaluation of Clinical Efficacy and Safety of Aortal Stent-Graft Created Using 3D Printing Technology","Evaluation of Clinical Efficacy and Safety of Aortal Stent-graft Modelled Printing 3D Model Printing Technology - Multicenter, Randomized Clinical Trial","Inclusion Criteria:\n\nFemale and male subjects age ≥ 18 2. Subject need to meet one of the following criteria:\n\n* Subjects with juxtarenal or suprarenal abdominal aortic aneurysm, type IV thoracoabdominal aneurysm of diameter \\>5.5cm (male) and 5.2cm (female)\n* Subjects with juxtarenal or suprarenal abdominal aortic aneurysm, type IV thoraco-abdominal aneurysm with aneurysm growth rate ≥ 0.5cm during 6 months\n* Type IA endoleak of post-implantation of abdominal stent- graft 3. Iliac arteries morphology with aortic stent graft implantation to be restored 4. Aortic segment which is proximal to aneurysm\n* Length ≥20mm\n* Diameter 20mm-36mm\n* Aortic suprarenal angle ≤75 degrees 5. Survival \\> 2 years\n\nExclusion Criteria:\n\n1. Female and male subjects age \\\u003C18\n2. Pregnancy and breast feeding\n3. Allergy and hypersensitivity to matherials of which the stent- graft is composed\n4. Hypersensitivity and contraindication to anti coagulation or contrast application to angio - CT which cannot be eliminated medically\n5. Coagulopathy which cannot medically treated\n6. Active infection which might cause stent - graft infection\n7. Creatinine level \\> 3.0mg\u002FdL\n8. Marphan syndrome, Ehlers - Denlos syndrome\n9. Unstable angina pectoris\n10. Raptured aortic aneurysm caused by cardiac insufficiency\n11. Unwillingness to comply with protocol procedures\n12. Iliac arteries morphology adequate for stent-graft implantation\n13. The diameter of the aortic flow lumen in reno-visceral aorta greater than 34mm\n14. Aortic section which is proximal to celiac artery with significant number of thrombi, calcification or changed by aneurysm\n15. Aorta with significant number of irregular thrombi which may lead to embolism (\"shaggy aorta\")\n16. Diameter of proximal kidney arteries which is exercisable to stenting \\\u003C4.5mm\n17. Devision of kidney artery which is exercisable to stenting in the distance of \\\u003C1cm of celiac artery, each of them is is in \\\u003C4.5mm in diameter\n18. Atypical anatomy of celiac artery in the form of separate exit of splenic and hepatic aortic artery",{"count":54,"type":20},100,[23],"the comparison of physician-modified stent-graft created in 3D models versus custom-made devices in the treatment of complex abdominal aortic aneurysm",[58,26,59,60,61],"Abdominal Aortic Aneurysm","Pararenal Abdominal Aortic Aneurysm","Thoracoabdominal Aortic Aneurysm","Type IA Endoleak",[63,64,65,66,29,67,68,69,70,71,30,72,73,74,75,76],"AAA","physician-modified stent-graft","custom-made device","complex abdominal aortic aneurysm","pararenal abdominal aortic aneurysm","thoracoabdominal aortic aneurysm","endovascular aneurysm repair","3D printing","3D model","type IA endoleak","aortic stent-graft","PMSG","patient-specific 3D model","complex aortic pathology","2026-04-13",{"date":79,"type":37},"2026-04-16",{"date":81,"type":37},"2022-11-01",{"date":83,"type":20},"2027-04-30",{"name":85,"class":44},"Samodzielny Publiczny Szpital Kliniczny nr 2 PUM"]