Now Available: Final Rule for FDAAA 801 and NIH Policy on Clinical Trial Reporting
3 studies found for:    15483279 [PUBMED-IDS]
Show Display Options
Rank Status Study
1 Enrolling by invitation Post-Market Study to Assess Outcomes of Patients Treated With AFX System Compared to Other EVAR Devices
Condition: Abdominal Aortic Aneurysm
Interventions: Device: AFX EVAR AAA Graft System;   Device: FDA Approved EVAR AAA Graft Systems
2 Unknown  Dutch Randomised Endovascular Aneurysm Management (DREAM-) Trial
Condition: Abdominal Aortic Aneurysm
Interventions: Procedure: Open Aneurysm Repair;   Procedure: Endovascular Aneurysm Repair
3 Recruiting Iliac Branch Excluder ReGistry (IceBERG)
Conditions: Abdominal Aortic Aneurysms;   Common Iliac Aneurysms;   Aneurysm
Intervention: Device: The Gore® EXCLUDER® ILIAC BRANCH Endoprosthesis.

Study has passed its completion date and status has not been verified in more than two years.