Dissecting aneurysm of the aorta Stanford classification, Aortic remodeling
Conditions
Interventions
Entry closure located at the orifice including the neck vessels, visceral arteries, and the iliac arteries.
Entry closure
Sponsors
Matsuda Hitoshi
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients who had past history of undergoing the surgery for aortic dissection. Patients who developed aortic dilation more than 45mm in thoracic aortic aneurysm or more than 40mm in abdominal aortic aneurysm. Patients who developed rapid aortic dilation more than 3mm in 6 months or more than 5mm in 12months.
Exclusion criteria
Exclusion criteria: Patients who had systemic infection that may increase the risk of device-related infection. Patients who are allergic to the material of the device. Pregnant women, lactating women or women who cannot agree on contraception during participating in this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Aortic diameter on CT at 12 months after intervention. | — |
Secondary
| Measure | Time frame |
|---|---|
| Occlusive condition of the false lumen 12 months after intervention. Aortic diameter on CT and occlusive condition of the false lumen 6 and 24 months after intervention. Freedom from aortic rupture, re-aortic dissection, sudden death, and secondary intervention | — |
Contacts
Public ContactYoshimasa Seike
National Cerebral and Cardiovascular Center
Outcome results
None listed