Drug-Eluting Balloons vs Mimetic Stents for Popliteal Artery Disease
Popliteal Arterial Stenosis
About this trial
This is an interventional treatment trial for Popliteal Arterial Stenosis focused on measuring Popliteal artery stenosis, Mimetic stent, Pharmacoactive balloon angioplasty, Chronic lower limb ischemia
Eligibility Criteria
Inclusion Criteria: Patients diagnosed of critical lower limb ischemia according to the TASC (TransAtlantic Inter-Society Consensus) working group. Patients admitted to the Vascular Surgery Department of the Bellvitge Hospital University to treat critical lower limb ischemia for endovascular treatment. With involvement of the Popliteal artery in-between the Hunter's canal and the start of the tibial artery branch. WOCBP must use highly effective methods of contraception. Patients who sign the written informed consent. Exclusion Criteria: Patients diagnosed of critical lower limb ischemia according to the TASC working group undergoing medical treatment or open surgery. Patients requiring amputation. Patients who underwent previous revascularization of the same limb (same artery). The main involvement is from an arterial territory other than the popliteal artery. Pregnant women. Inability of overcoming the arterial lesion during the endovascular procedure. Affected artery's diameter <4 mm.
Sites / Locations
- Hospital Universitari de BellvitgeRecruiting
Arms of the Study
Arm 1
Arm 2
Active Comparator
Experimental
Group A
Group B
Patients receiving pharmacoactive balloon angioplasty. Lutonix®
Patients receiving mimetic stent. Supera®