Lead Sponsor

Hospital St. Joseph, Marseille, France

Age

18 - No limit years

Sex

ALL

Healthy Volunteers

No

•Participant is willing and able to give informed consent for participation in the study.
•Male or Female, aged 18 years or above.
•Diagnosed with moderate to severe claudication: chronic symptomatic AOMI (Rutherford 2 and 3)
•Diagnosed with de novo obstructive lesions calcified in the superficial femoral artery or in P1: tight stenosis (\> 70%), calcified, layered, length ˃ 10 cm or short calcified occlusions \<5 cm from the superior femoral artery and P1.
•Able (in the Investigators opinion) and willing to comply with all study requirements.
•Willing to allow his or her General Practitioner and consultant, if appropriate, to be notified of participation in the study.
•Affiliated to social safety plan of beneficiary under such a plan

•Intra stent re-stenosis
•Recent occlusions, less than 1 month old of SFA and / or P1 (probable thrombus)
•SFA occlusion, P1 \> 5 cm, from origin of SFA.
•SFA stenosis \<10 cm
•Non calcified stenosis
•Participants who have participated in another research study involving an investigational product in the past 12 weeks
•Participant issuing with a safeguard measure of justice (in accordance with the low article L1122-2 of the public health code)