False lumen interventio
Not Applicable
- Conditions
- Dissecting aneurysm of the aortaStanford classification, Aortic remodelingI710
- Registration Number
- JPRN-jRCTs052190096
- Lead Sponsor
- Matsuda Hitoshi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- All
- Target Recruitment
- 15
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
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.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method