Purpose of this Study
We are doing this to study to test how well an investigational technology called the Endospan NEXUS Aortic Arch Stent Graft System (the study device) performs in the treatment of aortic arch disease.
Who Can Participate?
Eligibility
Adults ages 18+ who are diagnosed with aortic arch disease and plan to have surgery.
For more information about who can join this study, please contact the study team at susan.hajmohammad@duke.edu.
For more information about who can join this study, please contact the study team at susan.hajmohammad@duke.edu.
What is Involved?
If you choose to join this study, you will:
- Have your aorta repaired using the study device
- Have 9 CT scans
- Have 2 ultrasounds
- Have neurological assessments
- Fill out study questionnaires
- Have check-ups with the study team for up to 5 years after your aortic repair surgery
- Have your aorta repaired using the study device
- Have 9 CT scans
- Have 2 ultrasounds
- Have neurological assessments
- Fill out study questionnaires
- Have check-ups with the study team for up to 5 years after your aortic repair surgery
Study Details
Full Title
A Multi-arm, Multi-Center, Non-Randomized, Prospective, Clinical Study to Evaluate the Safety and Effectiveness of the NEXUS™ Aortic Arch Stent Graft System in Treating Thoracic Aortic Lesions Involving the Aortic Arch
Principal Investigator
George
Hughes
Protocol Number
PRO00107432
NCT ID
NCT04471909
Phase
N/A
Enrollment Status
OPEN TO ACCRUAL