I79.2
Conditions
Interventions
Group 1: Patients with chronic occlusion of the superficial femoral artery who underwent antegrade recanalisation.
The occlusion of the superficial femoral artery is confirmed during peripheral angiog
Sponsors
GRN Klinik Weinheim
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients who were referred to our department for endovascular treatment of femoropopliteal lesions due to claudication or critical limb ischemia
Exclusion criteria
Exclusion criteria: Patients with acute or subacute limb ischemia, Patients with non-occlusive lesions, Patients with occlusive lesions in less than 2 femoropopliteal vessel segments or occlusive lesions with only mild or no calcification, Patients with restenosis or occlusions in regions with previous implanted stents, Patients with occlusion length<10 cm.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint is vessel patency at 6 month follow-up (clinical evaluation). The primary endpoint will be assessed at 6 months after the intervention. The primary endpoint will be assessed through an interview by telephone. The patient will be asked if: - pain is present when walking - after how many meters does the pain start - is there an improvement - if wounds were present before the intervention, are the wounds closed - another intervention was necessary in the last 6 months (either endovascular or surgical) - a leg amputation occured | — |
Secondary
| Measure | Time frame |
|---|---|
| procedural time, radiation exposure and contrast agent administration, number and total length of implanted stents, peri- and postprocedural complications | — |
Countries
Germany
Contacts
Public ContactGrigorios Korosoglou
Department of Cardiology, Angiology and Pneumology GRN Klinik Weinheim
Outcome results
None listed