SIGNATURE Study : DCB (Legflow) vs POBA in Fempop Arteries

Cardionovum

Status

Enrolling

Conditions

Superficial Femoral Artery Stenosis

Angiopathy, Peripheral

Peripheral Arterial Disease

Study type

Observational

Funder types

Other

Industry

Identifiers

NCT04971772

FCRE-210621

Details and patient eligibility

About

The aim of this study is to demonstrate the superiority in safety and efficacy of the Legflow DCB vs standard uncoated POBA in a randomized controlled (RCT) for treatment of patients with symptomatic peripheral artery disease (PAD) due to stenosis, restenosis or occlusion of the femoral and/or popliteal arteries.

Enrollment

148 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria

Patient is ≥18 years
Patient has Rutherford Classification 2,3 or4.
Patient has provided written informed consent and is willing to comply with study follow-up requirements.
De novo stenotic or occlusive lesion(s) or non-stented restenotic or occlusive lesion(s) occurring >90 days after prior plain old balloon (POBA) angioplasty or >180 days after prior DCB treatment.
Target lesion is located between the ostium of the SFA and the end of the P1 segment of the popliteal artery
Target vessel diameter ≥ 4 mm and ≤ 7 mm
Target lesion must be stenotic or occlusive lesion ≤ 150mm in length (one long lesion or tandem lesions) by investigator's visual estimate. [Note: tandem lesions must have a total length of ≤ 150 mm by visual estimate and be separated by ≤ 30 mm.]
Target lesion must have angiographic evidence of ≥ 70 % stenosis by investigator's visual estimation
Successful, uncomplicated crossing of the target lesion occurs when the tip of the guidewire is distal to the target lesion without the occurrence of flow-limiting dissection of perforation and is judged by visual inspection to be within the true lumen. Subintimal dissection techniques may be used if re-entry occurs above-the-knee (ATK) and without the use of re-entry devices.
Target lesion is located at least 30mm from any stent if target vessel was previously stented.
A patent inflow artery free from significant stenosis ((≥50% stenosis) as confirmed by angiography.
At least one patent native outflow artery to the ankle or foot, free from significant stenosis (≥ 50 % stenosis) as confirmed by angiography.

Exclusion criteria:

Acute Limb Ischemia
Patient underwent an intervention involving the target vessel within the previous 90 days.
Patient underwent any lower extremity percutaneous treatment in the ipsilateral limb using plain old balloon (POBA) angioplasty within the previous 90 days.
Patient underwent a percutaneous transluminal angioplasty (PTA) of the target lesion using a DCB within the previous 180 days.
Pregnant women or women who are intending to become pregnant.
Patient has a life expectancy of less than 1 year
Patient has a known allergy to contrast medium that cannot be adequately pre-medicated.
Patient is allergic to all anti-platelet treatments
Patient is receiving immunosuppressant therapy
Patient has platelet count <100.000/mm3 or >700.000/mm
Patient has history of gastrointestinal hemorrhage requiring a transfusion within 3 months prior to the study procedure
Patient is diagnosed with coagulopathy that precludes treatment with systemic anticoagulation and/or dual antiplatelet therapy (DAPT)
Patient has history of stroke within past 90 days
Patient has history of myocardial infarction within the past 30 days.
Patient is participating in an investigational drug or medical device study that has not completed primary endpoint(s) evaluation or that clinically interferes with the endpoints from this study.
Patient has had any major (e.g. cardiac, peripheral, abdominal) surgical procedure or intervention unrelated to this study within 30 days prior to the index procedure or has planned major surgical procedure or intervention within 30 days of the index procedure
An intervention in the contralateral limb, planned within 30 days post-index procedure
Patient had previous bypass surgery of the target lesion
Patient had previous treatment of the target vessel with thrombolysis or surgery
Patient is unwilling or unable to comply with procedures specified in the protocol or has difficulty or inability to return for follow-up visits as specified by the protocol
Target lesion involves an aneurysm or is adjacent to an aneurysm (within 5 mm)
Target Lesion requires treatment with alternative therapy such as stenting, laser, atherectomy, cryoplasty, brachytherapy or re-entry devices
Significant target vessel tortuosity or other parameters prohibiting access to the target lesion
Presence of thrombus in the target vessel
Iliac inflow disease requiring treatment, unless the iliac artery disease is successfully treated first during the index procedure. Success is defined as ≤ 30 % residual diameter stenosis without death or major complications.
Presence of an aortic, iliac or femoral artificial graft.