Aortic Aneurysm, Thoracic, Aortic Dissection
Conditions
Keywords
endograft
Brief summary
Multicenter registry on patients treated by the new Gore thoracic branched endoprosthesis
Detailed description
This is a multicenter, non-sponsored, physician-initiated multicenter registry on patients treated with the Gore thoracic branched endoprosthesis. Inclusion of centers is on a voluntary basis; each participating center includes consecutive patients treated with this device.
Interventions
DEVICEGORE TAG Thoracic Branch Endoprosthesis
deployment of the GORE TAG Thoracic Branch Endoprosthesis fro thoraci aorta pathologies
Sponsors
University Hospital Padova
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* patients receving the Gore TAG thoracic branched endograft for thoracic aorta pathologies
Exclusion criteria
* less than 18 years * allergy to endograft components * patients receiving other types of arch endografts
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| early mortality | 30 days | mortality related to the intervention within 30 days |
| device stability | 5 years | freedom from related mortality, reintervention, type 1a endoleak during follow-up |
| technical success | 30 days | succesful deployment of all endograft components at the intended site with complete aneurysm exclusion, without surgical conversion, type Ia/III endoleak, kink, stenosis, graft occlusion |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| early major adverse events | 30 days | stroke, spinal cord ischemia, vascular complications, cardiac complications, respiratory insufficiency, early reintervention, acute kidney injury |
Countries
Italy
Contacts
Primary ContactMichele Antonello, PhD
Outcome results
None listed