This is a multicentric voluntary observational study with a retrospective evaluation of prospectively collected data concerning the treatment of visceral aneurysms with flow diversion stent Derivo Peripher and Derivo 2 (DED, Acandis GmbH) Follow-up will include clinical and radiological (CT) evaluation at least 12 months after the intervention. The enrollment period will be of 65 months (01/jan/2020-30/jun/2025). Sample size will be of 100 patients.
Age range
18 Years
Sex
ALL
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The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Efficacy of the stenting in terms of patency and side branches
Timeframe: 12 months
Efficacy of the stenting in terms of aneurysm thrombosis rate
Timeframe: 12 months
Efficacy of the stenting in terms of aneurysm volume assessment
Timeframe: 12 months
Safety in terms of morbidity
Timeframe: 12 months
Safety in terms of mortality
Timeframe: 12 months
Safety in terms of technical issues
Timeframe: 12 months