TiGER-001
- Study HIC#:2000030522
- Last Updated:11/12/2025
The purpose of this study is to better understand how the study device performs. This study will collect information about your procedure, how well the study device performs after your procedure and will also collect information about your physical and emotional wellbeing both before and after your procedure. The information collected during the study will help to give study doctors and the study device manufacturer feedback on the long-term safety and performance of all Terumo Aortic devices. Information is being collected from approximately 1000 subjects around the world.
In the United States of America (USA), only subjects who would be routinely given a Terumo Aortic RelayPro Thoracic Stent-Graft System to treat a lesion in your descending thoracic aorta can participate in this study. The study will not require you to have any additional medical or surgical procedures beyond those that you will have to treat your condition.
Contact Us
For more information about this study, including how to volunteer, contact:
Wasima Shinwari
- Phone Number: 1-518-414-0322
Help Us Discover!
You can help our team find trials you might be eligible for by creating a volunteer profile in MyChart. To get started, create a volunteer profile, or contact helpusdiscover@yale.edu, or call +18779788343 for more information.
Eligibility Criteria
- Minimum age as per local regulations
- Indication for aortic endovascular repair with an approved or CE marked by a Regulatory body or custom-made Terumo Aortic Endovascular graft
- Ability to provide informed consent
- Emergent cases (typically younger patients with traumatic injuries) are not excluded if there is IRB/EC agreement to allow consent after intervention (i.e. consent to study participation, not to treatment)
- Willingness to comply with the registry protocol
- Willingness to adhere to follow-up visits
