Clinical Trial Investigating the Efficacy of the Supera Peripheral Stent System for the Treatment of the Common Femoral Artery (VMI-CFA)

ID3 Medical

Status

Completed

Conditions

Peripheral Arterial Disease

Treatments

Device: Supera Peripheral Stent System

Study type

Interventional

Funder types

Other

Identifiers

NCT02804113

iD3 Medical - 160226

Details and patient eligibility

About

The VMI-CFA study investigates the efficacy of the Supera Stent in the treatment of common femoral artery stenosis or occlusion. 100 patients will be included with a RF of 2 to 4. The lesion is located within the native CFA and treated with predillation prior to stenting with the Supera Peripheral Stent System. Patients will be invited for a follow-up visit at 1, 6, 12 and 24 month post procedure. The primary endpoint of the study is the primary patency at 12 months and periprocedural events up to 30 days post procedure. Secondary endpoints include technical success, primary patency rate at 1, 6 and 24 month, freedom from TLR at 1-, 6-, 12 and 24 month follow-up and clinical success at 1-, 6-, 12- and 24-month follow-up.

Enrollment

100 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patient presenting a score from 2 to 4 following Rutherford classification
Patient is willing to comply with specified follow-up evaluations at the specified times
Patient is >18 years old
Patient understands the nature of the procedure and provides written informed consent, prior to enrolment in the study
Patient has a projected life expectancy of at least 12 months
Prior to enrolment, the guidewire has crossed target lesion
De novo lesions located in the common femoral artery, suitable for endovascular therapy
The target lesions are located within the native CFA: localized between the origin of the circumflex iliac artery and the proximal (1cm) superficial femoral artery.
There is angiographic evidence of a patent deep femoral artery
The target lesion has angiographic evidence of stenosis > 50% or occlusion
There is angiographic evidence of at least one-vessel-runoff to the foot, irrespective of whether or not outflow was re-established by means of previous endovascular intervention

Exclusion criteria

Presence of another stent in the target vessel that was placed during a previous procedure
Previous open surgery in the same limb
Patients contraindicated for antiplatelet therapy, anticoagulants or thrombolytics.
Patients who exhibit persistent acute intraluminal thrombus at the target lesion site.
Perforation at the angioplasty site evidenced by extravasation of contrast medium
Patients with known hypersensitivity to nickel-titanium and heparin, including those patients who have had a previous incidence of heparin-induced thrombocytopenia (HIT) type II
Patients with uncorrected bleeding disorders
Female patient with child bearing potential not taking adequate contraceptives or currently breastfeeding
Ipsilateral inflow (aorto-iliac) artery treatment before target lesion treatment with a residual stenosis>30%
Use of thrombectomy, atherectomy or laser devices during procedure
Any planned surgical intervention/procedure 30 days after the study procedure
Any patient considered to be hemodynamically unstable at onset of procedure
Patient is currently participating in another investigational drug or device study that has not reached the primary endpoint.
Severe medical comorbidities (untreated CAD/CHF, severe COPD, metastatic malignancy, dementia, etc.) or other medical condition that would preclude compliance with the study protocol or 1-year life expectancy
Major distal amputation (above the transmetatarsal) in the study limb or non-study limb
Septicemia or bacteremia
Known allergy to contrast media that cannot be adequately pre-medicated prior to the study procedure