Clinical Study of Thoracic Endovascular Repair for Aortic Arch Aneurysms with Surgeon-Modified Fenestrated and Retrograde Branched Device
Not Applicable
- Conditions
- Aortic Arch or Distal Arch Aneurysms
- Registration Number
- JPRN-UMIN000020057
- Lead Sponsor
- Shimane Prefectural Central Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 15
Inclusion Criteria
Not provided
Exclusion Criteria
<General Exclusion Criteria> 1) Less than 20 years of age 2) Pregnant or patients likely to have been pregnant 3) Life expectancy less than 1 years 4) Unwilling to company with the follow up schedule 5) Inability or refusal to give informed consent *Additionally, there is Medical Exclusion Criteria and Anatomical Exclusion Criteria, too.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The rates of aortic disease related death at 12 months post-procedure
- Secondary Outcome Measures
Name Time Method Device Success, Procedural Time, Condit Usage During The Procedure, Clinical Utility Measures, Morbidity, Including The Composite Rate Of Major Adverse Events, Endoleak, Change In Aneurysm Size, Migration, Device Patency, Device Integrity