Overview
The goal of this registry is to evaluate the semibranch in branched endovascular aortic repair, which is a new tool in endovascular branched aortic repair.
Description
The main question it aims to answer are:
- Patency of the semibranch
- Feasibility of the technique regarding cannulation and stentgrafting
The participants will treated with the custom made semibranch device and enrolled in the registry if they consent. No change in treatment will be made when enrolled.
Eligibility
Inclusion Criteria:
- 18 years or older
- Presence of pararenal or thoracoabdominal aortic pathology
- Treatment planned a semibranch device branch from Artivion
- Availability of the patients during the follow up period
- Informing patients about the study and providing written informed consent
Exclusion Criteria:
- Women of childbearing age
- Patients under 18 years