I71.4
Conditions
Interventions
Group 1: Study participants with abdominal aortic aneurysm will be examined once before and after intervention using the specially developed BioScanRack, a non-contact technique that measures the pusl
Sponsors
Klinik und Poliklinik für Vaskuläre und Endovaskuläre Chirurgie
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: -Capable of giving consent -Patients with abdominal aortic aneurysm (Dmax men = 5,5 cm, Dmax women = 5,0 cm) -Patients without aortic pathologies -BMI < 35
Exclusion criteria
Exclusion criteria: - Patients with acute symptomatic BAA - Patients with condition after stenting or open interventions in the area of the iliac arteries and thoracic aorta - Patients with concomitant aneurysms of the iliac arteries - Patients for whom written information is not possible - Vulnerable population
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The measurement of aortas and aortic aneurysms (maximum diameter, pressure in the aneurysm sac) using the specially developed BioScanRack before and after intervention in study participants with aortic aneurysms and once in study participants without aortic pathologies. | — |
Secondary
| Measure | Time frame |
|---|---|
| The measurement of thrombus, endoleaks and vascular calcification. | — |
Countries
Germany
Contacts
Public ContactDaniela Branzan
Klinik und Poliklinik für Vaskuläre und Endovaskuläre Chirurgie
Outcome results
None listed