The purpose of this post-approval study is to evaluate the long-term performance of the GORE TAG® Thoracic Endoprosthesis (TAG device) in the primary treatment of descending thoracic aortic (DTA) aneurysms
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
150
implant
Unnamed facility
Phoenix, Arizona, United States
Unnamed facility
Los Angeles, California, United States
Aneurysm Related Death
Freedom from aneurysm related mortality for TAG 05-02 subjects
Time frame: 5 years
A Subset of Major Adverse Events Will be Evaluated in Subjects Treated With the TAG Device and Subjects Treated With Open Surgical Repair.
Proportion of subjects in TAG 05-02 with MAEs
Time frame: 5 years
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Unnamed facility
San Francisco, California, United States
Unnamed facility
Greeley, Colorado, United States
Unnamed facility
Gainesville, Florida, United States
Unnamed facility
Miami, Florida, United States
Unnamed facility
Chicago, Illinois, United States
Unnamed facility
Peoria, Illinois, United States
Unnamed facility
Kansas City, Kansas, United States
Unnamed facility
New Orleans, Louisiana, United States
...and 15 more locations