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.

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.

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

Patients with pararenal or thoracoabdominal aortic pathology, who are treated with a endovascular semibranch stentgraft.