Aortal occlusive disease
Conditions
Interventions
Group 1: Patients with interventions of the abdominal aorta or the aorta involving the iliac arteries who were treated at the University Medical Centre Freiburg at the University Heart Centre on the B
Sponsors
Universitätsklinik Freiburg
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients with interventions of the abdominal aorta or the aorta involving the iliac arteries who were treated at the University Medical Centre Freiburg at the University Heart Centre on the Bad Krozingen campus
Exclusion criteria
Exclusion criteria: - Patients who have not been treated aortally or aorto-iliacally - Patients who have undergone interventional treatment due to an aneurysm of the aorta or the aorta involving the iliac arteries.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Acute intervention success, defined as <30% residual stenosis | — |
Secondary
| Measure | Time frame |
|---|---|
| - Freedom from re-intervention at the target lesion (target lesion revascularisation, TLR) after 12, 24, 36, 38 and 60 months - Restenosis rate after 12, 24, 36, 38 and 60 months - Change in the Rutherford-Becker classification after 12, 24, 36, 38 and 60 months - Amputation rate after 12, 24, 36, 38 and 60 months - Death rate after 12, 24, 36, 38 and 60 months | — |
Countries
Germany
Contacts
Public ContactThomas Zeller
Universitätsklinik Freiburg
Outcome results
None listed