At a glance
ClinicalIndex Comparison RecordPhase 2Completed· 35 enrolled
Drug / intervention
31 mm GORE EXCLUDER® AAA Endoprosthesisdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Clinical Study Evaluating the Use of the GORE EXCLUDER® AAA Endoprosthesis - 31mm In the Primary Treatment of Infrarenal Abdominal Aortic Aneurysms
In Brief
A Phase 2 clinical trial evaluating 31 mm GORE EXCLUDER® AAA Endoprosthesis for Aortic Aneurysm, Abdominal. Completed, enrolled 35 participants across 1 site.
Detailed Summary
The purpose of this study is to assess the safety and efficacy of the 31 mm GORE EXCLUDER® AAA Endoprosthesis in the treatment of infrarenal abdominal aortic aneurysms
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsAortic Aneurysm, Abdominal
CountriesUnited States
Collaborators--
Timeline
Phase 2CompletedFinished
2006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
Enrollment StartMay 2006
First PostedFeb 2008
Primary CompletionMar 2008
Study CompletionJun 2014
TodayJul 2026
First PostedFeb 14, 2008
Enrollment StartMay 1, 2006
Primary CompletionMar 1, 2008
Study CompletionJun 1, 2014
TodayJul 2, 2026
Enrollment to primary: 1.8 yearsPosted 18.4 years ago
Interventions
31 mm GORE EXCLUDER® AAA Endoprosthesisdevice
GORE EXCLUDER® AAA Endoprosthesis - 31 mm device implanted for the primary treatment of infrarenal abdominal aortic aneurysms (AAA)