Clinical Trials Logo

Aortoiliac Aneurysms clinical trials

View clinical trials related to Aortoiliac Aneurysms.

Filter by:
  • None
  • Page 1

NCT ID: NCT02571907 Completed - Iliac Aneurysms Clinical Trials

PRESERVE-Zenith® Branch Endovascular Graft-Iliac Bifurcation Clinical Study

Start date: April 1, 2014
Phase: N/A
Study type: Interventional

The purpose of this extended study is to evaluate the safety and effectiveness of the Zenith® Branch Endovascular Graft-Iliac Bifurcation in combination with the commercially available Atrium iCAST™ covered stent in patients in a treatment of aortoiliac and iliac aneurysms.

NCT ID: NCT02535065 Completed - Clinical trials for Abdominal Aortic Aneurysms

Zenith® Low Profile AAA Endovascular Graft

Start date: August 2014
Phase: N/A
Study type: Interventional

The Zenith® Low Profile AAA Endovascular Graft Clinical Study is a clinical trial to study the safety and effectiveness of the Zenith® Low Profile AAA Endovascular Graft used in conjunction with the Zenith® Spiral-Z® AAA Iliac Leg Graft to treat abdominal aortic, aortoiliac, and iliac aneurysms.

NCT ID: NCT02475798 No longer available - Iliac Aneurysms Clinical Trials

PRESERVE-Zenith® Branch Endovascular Graft-Iliac Bifurcation

Start date: n/a
Phase:
Study type: Expanded Access

The purpose of this extended study is to collect confirmatory safety and effectiveness data on the Zenith® Branch Endovascular Graft-Iliac Bifurcation in combination with the commercially available Atrium iCAST™ covered stent in the treatment of aortoiliac and iliac aneurysms.

NCT ID: NCT02087501 Completed - Clinical trials for Aortoiliac Aneurysms

HORIZON CE Pivotal Study to Treat Abdominal Aortic Aneurysm

Start date: April 2014
Phase: N/A
Study type: Interventional

Clinical Investigation Design A prospective, open-label, non-randomized, interventional clinical study, sponsored by Endospan Ltd. Patients will be followed-up for five years. Investigational Device The Horizon™ Abdominal Aortic Aneurysm Stent Graft System and its designated Delivery System. Purpose The purpose of the study is to evaluate the safety and performance of the Horizon™ AAA Stent Graft System for the treatment of infrarenal abdominal aortic and/or aortoiliac aneurysms. The results of this study will be used as supportive data for CE Marking submission in the European Union (EU). Objectives The primary objectives of the study are to evaluate the safety and performance of the Horizon™ AAA Stent graft System. Primary End Points Safety endpoints include proportion of patients free from device related Major Adverse Events (MAEs) within 1 month of the endovascular procedure. Performance endpoints include successful delivery and deployment of the device; and absence of the following at 1 month follow-up: aneurysm growth ≥5mm, type I or III endoleaks, stent graft occlusion, conversion to open surgery, rupture and stent graft migration. Subject population Thirty (30) patients having infrarenal abdominal aortic and/or aortoiliac aneurysms, having Iliac/femoral access vessel morphology that is compatible with vascular access techniques and devices. Treatment All patients will be treated by implantation of the Horizon™ Abdominal Aortic Aneurysm Stent graft System.