Clinical trials: Aorto Iliac Aneurysm
Aortic Aneurysm
Abdominal Aortic/Aorto-Iliac Aneurysm Endoluminal Graft Study
The Bifurcated PowerLink System is intended to provide a permanent alternative conduit for blood flow within a patient's abdominal vascular system, which excludes the aneurysmal sac from blood flow and pressure.
- Trial name
- NCT00549354
- Testing
- Endoluminal Graft
- Where
- United States
- Volunteers
- 34 people
- Sponsor
- Arizona Heart Institute
Abdominal Aortic Aneurysms, Aorto-iliac Aneurysms
Zenith® Fenestrated Abdominal Aortic Aneurysm (AAA) Endovascular Graft Continued Access Study
The Zenith®Fenestrated AAA Endovascular Graft Clinical Study is a clinical investigation approved by the US FDA to study the safety and effectiveness of the Zenith® Fenestrated AAA Endovascular Graft in the treatment of abdominal…
- Conditions
- Abdominal Aortic Aneurysms, Aorto-iliac Aneurysms, Juxtarenal Aneurysms
- Trial name
- NCT02577562
- Testing
- Zenith® Fenestrated AAA Endovascular Graft
- Where
- 15 sites in United States
- Sponsor
- Cook Group Incorporated
Abdominal Aortic Aneurysms, Aorto-iliac Aneurysms
Zenith(R) Fenestrated Abdominal Aortic Aneurysm (AAA) Endovascular Graft Clinical Study
The Zenith(R) Fenestrated AAA Endovascular Graft Clinical Study is a clinical investigation approved by the US FDA to study the safety and effectiveness of the Zenith(R) Fenestrated AAA Endovascular Graft in the treatment of…
- Conditions
- Abdominal Aortic Aneurysms, Aorto-iliac Aneurysms, Juxtarenal Aneurysms
- Trial name
- NCT00875563
- Testing
- Zenith(R) Fenestrated AAA Endovascular Graft
- Where
- 14 sites in United States
- Volunteers
- 42 people
- Sponsor
- Cook Group Incorporated
Aorto-iliac Aneurysm
Evaluation Of Cost-Effectiveness Of Iliac Branch Endoprostheses
The study is a multi-center, voluntary observational study on an ambispective cohort of patients treated between January 2018 and December 2025.The study aims to enroll 300 patients (around 200 patients in the retrospective…
- Trial name
- ECO-IBE (NCT07096388)
- Testing
- endovascular repair, open surgical repair
- Where
- Italy
- Volunteers
- 300 people
- Sponsor
- Prof. Andrea Kahlberg
Abdominal Aortic Aneurysm
ARBITER-II: Aorfix™ Bifurcated Safety and Performance Trial: Phase II, Angulated Vessels
To assess the safety and performance of Aorfix™ Stent Grafts in the treatment of Abdominal Aortic and Aorto-Iliac Aneurysm where a significant degree of vessel angulation exists at the neck of the aneurysm or in the common iliac…
- Trial name
- ARBITER-II (NCT00442065)
- Testing
- Aorfix™ Stent Grafts (AAA endovascular procedure)
- Where
- 6 sites in Czechia, Germany and 3 more
- Volunteers
- 30 people
- Sponsor
- Lombard Medical
Aortic Aneurysm, Abdominal, Aorto Iliac Aneurysm
The STAPLE International Post-Market Registry
The Aptus Endosystems STAPLE International Post-Market Registry is intended to expand the clinical knowledge base by including 'real world' subjects.
- Trial name
- NCT01276249
- Testing
- Fortevo Endograft
- Where
- 9 sites in Canada, Germany and 4 more
- Volunteers
- 108 people
- Sponsor
- Medtronic Cardiovascular
Endovascular
Evaluation of the Clinical and Cost-effectiveness of an Automated Mobile Hybrid Room in Vascular Surgery Compared with Current Practice
Evaluation of the clinical and cost-effectiveness of a mobile hybrid room compared with current practice without mobile hybrid room and imaging fusion guidance, in a French multicentre clinical setting.
- Trial name
- RADIOPROTEC (NCT06590532)
- Testing
- Endovascular aneurysm repair or aorto iliac endovascular revascularisation with Fusion imaging system Cydar-EV, Endovascular aneurysm repair or aorto iliac endovascular revascularisation without Fusion imaging system Cydar-EV
- Where
- 7 sites in France
- Volunteers
- 350 people
- Sponsor
- Nantes University Hospital
Aorto-iliac Occlusive Disease (AIOD), Visceral Artery Occlusive Disease (VAOD)
GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis Post-Market Clinical Follow-Up (PMCF) Observational Registry (RE-PROVE)
Collect real-world post-market clinical follow-up data on subjects treated with the Reduced Profile GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis (Reduced Profile VBX Stent Graft-BXB)
- Conditions
- Aorto-iliac Occlusive Disease (AIOD), Visceral Artery Occlusive Disease (VAOD), Isolated Artery Aneurysms (IAA), Trauma or Iatrogenic Vessel Injury
- Trial name
- NCT07279649
- Testing
- Reduced Profile GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis (Reduced Profile VBX Stent Graft-BXB)
- Where
- Germany
- Volunteers
- 240 people
- Sponsor
- W.L.Gore & Associates
Abdominal Aortic Aneurysm
Post-Approval Study of the TREO Abdominal Stent-Graft System
The purpose of this study is to determine the long-term performance of the TREO Abdominal Stent-Graft as a treatment for patients with Infrarenal Abdominal Aortic Aneurysms or Aorto-iliac Aneurysms.
- Trial name
- TREO PAS (NCT04697784)
- Testing
- TREO Abdominal Stent-Graft System
- Where
- 40 sites in United States
- Volunteers
- 338 people
- Sponsor
- Bolton Medical
Abdominal Aortic Aneurysm, Aorto-iliac Aneurysm
Zenith® LP Abdominal Aortic Aneurysm (AAA) Post-Market Registry
A registry to collect additional prospective intra-operative and follow-up information on physician use of the CE-marked Zenith® Low Profile Abdominal Aortic Aneurysm (AAA) Endovascular Graft under routine clinical care.
- Trial name
- NCT01424267
- Testing
- Zenith® Low Profile AAA Endovascular Graft
- Where
- 15 sites in Austria, Germany and 5 more
- Volunteers
- 76 people
- Sponsor
- Cook Group Incorporated
Abdominal Aortic Aneurysm (AAA), Aorto-iliac Aneurysm
Fenestrated AAA Endovascular Graft Post-Approval Study
This post-market study is approved by the US FDA to evaluate the long-term safety and performance of the Zenith® Fenestrated AAA Endovascular Graft.
- Conditions
- Abdominal Aortic Aneurysm (AAA), Aorto-iliac Aneurysm, Juxtarenal Aneurysm
- Trial name
- NCT01990950
- Testing
- Zenith® Fenestrated AAA Endovascular Graft
- Where
- 6 sites in United States
- Volunteers
- 21 people
- Sponsor
- Cook Research Incorporated
Aortic Aneurysm, Iliac Aneurysm
Comparison of Aorto-iliac Endovascular Interventions With and Without the EndoNaut Workstation
The aim of this retrospective, multicenter study is to demonstrate that the use of EndoNaut for aortoiliac endovascular procedures has a clinical impact for the patient (reduction in irradiation and the volume of contrast…
- Conditions
- Aortic Aneurysm, Iliac Aneurysm, Stenoses, Aortic, Iliac Artery Stenosis
- Trial name
- COM-ENDO (NCT04714268)
- Testing
- Aorto-iliac endovascular procedure
- Where
- France
- Volunteers
- 150 people
- Sponsor
- Therenva
Abdominal Aortic, Aorto-iliac Aneurysm
Zenith Alpha™ Abdominal Endovascular Graft
The purpose of this study is to evaluate the clinical performance of the Zenith Alpha™ Abdominal Endovascular Graft for the treatment of abdominal aortic or aorto-iliac aneurysm.
- Trial name
- NCT03061825
- Testing
- Zenith Alpha™ Abdominal Endovascular Graft
- Where
- 5 sites in Canada
- Volunteers
- 100 people
- Sponsor
- Cook Research Incorporated
Abdominal Aortic Aneurysms, Iliac Aneurysms
Zenith(R) Low Profile AAA Endovascular Graft Clinical Study
The Zenith® Low Profile AAA Endovascular Graft Clinical Study is a clinical trial approved by US FDA to study the safety and effectiveness of the Zenith® Low Profile AAA Endovascular Graft to treat abdominal aortic, aorto-iliac…
- Conditions
- Abdominal Aortic Aneurysms, Iliac Aneurysms, Aorto-iliac Aneurysms
- Trial name
- NCT00833924
- Testing
- Zenith(R) Low Profile AAA Endovascular Graft
- Where
- 27 sites in United States, China and 3 more
- Volunteers
- 120 people
- Sponsor
- Cook Group Incorporated
Aorto-iliac Aneurysms, Iliac Aneurysms
PRESERVE-Zenith® Iliac Branch System Clinical Study
The PRESERVE-Zenith® Iliac Branch System Clinical Study is a clinical trial to study the safety and effectiveness of the Zenith® Branch Endovascular Graft-Iliac Bifurcation in combination with the Zenith® Connection Endovascular…
- Trial name
- NCT01208415
- Testing
- Endovascular repair for aortoiliac or iliac aneurysms.
- Where
- 19 sites in United States
- Volunteers
- 40 people
- Sponsor
- Cook Group Incorporated
Abdominal Aortic Aneurysms, Iliac Aneurysms
Zenith® Low Profile AAA Endovascular Graft
This extended investigation is to provide continued physician access to the device and collect confirmatory safety and effectiveness data.
- Conditions
- Abdominal Aortic Aneurysms, Iliac Aneurysms, Aorto-iliac Aneurysms
- Trial name
- NCT02557659
- Testing
- Zenith Low Profile AAA Endovascular Graft
- Where
- 22 sites in United States
- Sponsor
- Cook Group Incorporated
Abdominal Aortic Aneurysm, Aorto-iliac Aneurysm
Zenith® Spiral-Z® AAA Iliac Leg Graft Post-market Registry
The purpose of this registry is to obtain case reports of physician experience with the Spiral-Z® graft under routine clinical care.
- Trial name
- NCT01540643
- Testing
- Iliac Leg Graft
- Where
- 31 sites in United States, Canada
- Volunteers
- 600 people
- Sponsor
- Cook Group Incorporated
Common Iliac Artery Aneurysm, Aorto Iliac Aneurysm
Assessment of GORE® EXCLUDER® IBE Plus Stent Graft Performance in Patients Undergoing Endovascular Iliac Revascularization
The IBE 25-05 study will be a prospective, non-randomized, multicenter, interventional two arm evaluation designed to assess the safety and effectiveness of the GORE® EXCLUDER® IBE Plus Stent Graft in patients with common iliac…
- Trial name
- NCT07304102
- Testing
- GORE® EXCLUDER® IBE Plus Stent Graft
- Volunteers
- 100 people
- Sponsor
- W.L.Gore & Associates
Aorto-iliac Aneurysms, Iliac Aneurysms
Zenith(R) Connection Endovascular Covered Stent Clinical Study
The Zenith(R) Connection Endovascular Covered Stent Clinical Study is a clinical investigation to study the safety and performance of the Zenith(R) Connection Endovascular Covered Stent in conjunction with the Zenith(R) Branch…
- Trial name
- NCT00893620
- Testing
- Zenith(R) Connection Endovascular Covered Stent with the Zenith® Branch Endovascular Graft-Iliac Bifurcation and Zenith Flex(R) AAA Endovascular Graft
- Where
- 4 sites in Germany, Hong Kong and 1 more
- Volunteers
- 1 people
- Sponsor
- Cook Group Incorporated
Peripheral Artery Disease, Abdominal Aortic Aneurysm
Endovascular Treatment of Aorto-iliac Disease Using in Situ Fenestration
In situ fenestration (ISF) could represent an alternative in the treatment of aorto-iliac disease when usual techniques are not available. The aim of this study was to present the results of ISF in aorto-iliac disease.
- Trial name
- PREFISIT (NCT04062734)
- Where
- France
- Volunteers
- 30 people
- Sponsor
- Assistance Publique - Hôpitaux de Paris