Abdominal aortic aneurysm, coil embolization
Conditions
Interventions
Group 1: Routine clinical data already collected from the Heidelberg patient collective will be catalogued and systematized.
Sponsors
Universitätsklinikum
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients who underwent implantation of a stent graft in the abdominal aorta (EVAR) between January 1, 2018 and December 31, 2023 at the Clinic for Vascular Surgery and Endovascular Surgery Heidelberg due to an abdominal aortic aneurysm, as well as patients who have already been included in the internal database of the Clinic for Vascular Surgery and Endovascular Surgery (S-583/2013).
Exclusion criteria
Exclusion criteria: Underage patients; discontinuation of study participation (S-583/2013) (leads to immediate anonymization of data)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The finalgoal is to evaluate the radiation exposure and intervention time during endovascular aneurysm repair (EVAR) with respect to the primary goal of reducing type 2 endoleak-associated complications in the postoperative course. | — |
Secondary
| Measure | Time frame |
|---|---|
| Investigation of the rate of endoleak type II, post-interventional aneurysm growth/shrinkage, recording of primary interventions and re-interventions, as well as analysis of morphological parameters of the vascular anatomy using CT morphological data in relation to technical success (which were collected as part of the clinical care of the patients) | — |
Countries
Germany
Contacts
Public ContactAlexandru Barb
Universitätsklinikum Heidelberg
Outcome results
None listed