Semibranch CMD branched aortic stentgraft: bEVAR with a custom made abdominal aortic multibranch, which incorporates the semibranch design
Study summary
The goal of this registry is to evaluate the semibranch in branched endovascular arotic repair, which is a new tool in endovascular branched aortic repair.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
* Patient has been treated with the semibranch stentgraft
* Patient is over 18 years old
Primary outcome measure(s)
Freedom from target vessel instability — 30 days after intervention Primary patency and freedom from stenosis of the semibranch
Mortality — 30 days after intervention Overall mortality rate during 30 days after intervention
Technical success — 12 hours after intervention cannulation and stentgrafting ot the semibranches
Trial sites (1)
Facility
City
Region
Status
Muenster University Hospital
Münster
Germany
Recruiting
More University Hospital Muenster trials in Germany
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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