Endurant Stent Graft System Post Approval Study (ENGAGE PAS)
|ClinicalTrials.gov Identifier: NCT01379222|
Recruitment Status : Active, not recruiting
First Posted : June 23, 2011
Last Update Posted : November 6, 2017
The purpose of the study is to demonstrate the long term safety and effectiveness of the Endurant Stent Graft System for the endovascular treatment of infrarenal abdominal aortic aneurysms in a post-approval environment, through the endpoints established in this protocol.
The clinical objective of the study is to evaluate the long term safety and effectiveness of the Endurant Stent Graft System assessed at 5 years through freedom from Aneurysm-Related Mortality (ARM).
|Condition or disease||Intervention/treatment||Phase|
|Aortic Aneurysm, Abdominal||Device: Endurant Stent Graft System||Not Applicable|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||178 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||Post Approval Study Evaluating the Long Term Safety and Effectiveness of the Endurant Stent Graft System (ENGAGE PAS)|
|Study Start Date :||August 2011|
|Actual Primary Completion Date :||September 2017|
|Estimated Study Completion Date :||March 2018|
Experimental: ENGAGE PAS De Novo Subjects
The Endurant Stent Graft System Bifurcated device is administered to patients diagnosed with an abdominal aortic or aortoiliac aneurysm who are considered candidates for endovascular repair, per the FDA approved Instructions For Use (IFU).
Device: Endurant Stent Graft System
The Endurant Stent Graft System is designed to treat infrarenal abdominal aortic aneurysms using an endovascular approach. When placed within the aneurysm, the Endurant Stent Graft is designed to provide a permanent, alternative conduit for blood flow within the patient's vasculature by excluding the aneurysmal sac from blood flow and pressure.
- Freedom from Aneurysm-related Mortality Rate (ARM) at 5 years (1826 days) [ Time Frame: 5 years ]
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01379222
|United States, Texas|
|Saint Luke's Episcopal Hospital-Texas Medical Center|
|Houston, Texas, United States, 77030|
|Principal Investigator:||Marc Schermerhorn, MD||Beth Israel Deaconess Medical Center|