PROMISE III: Percutaneous Deep Vein Arterialization for the Treatment of Late-Stage Chronic Limb-Threatening Ischemia

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-95
SponsorLimFlow, Inc.

About this trial

A prospective, single-arm, multi-center study designed to gather additional information on the LimFlow System.

Eligibility criteria

Qualifiers

Subject must be ≥ 18 and ≤ 95 years of age

Clinical diagnosis of chronic limb-threatening ischemia, defined as any of the following clinical assessments: previous angiogram or hemodynamic evidence of severely diminished arterial inflow of the index limb (e.g., ABI ≤ 0.39, TP / TcPO2 < 30 mm Hg) and

Rutherford Classification 5, ischemic ulceration or

Rutherford Classification 6, ischemic gangrene

Disqualifiers

Concomitant hepatic insufficiency, thrombophlebitis in the target limb, or non-treatable coagulation disorder within the past 90 days.

Active immunodeficiency disorder or currently receiving immunosuppressant therapy for an immunodeficiency disorder.

Prior peripheral arterial bypass procedure above or below the knee which would inhibit proximal inflow to the stent graft.

Absence of adequate viable tissue in target foot.

Trial design

Treatments tested in this trial

  • LimFlow Stent Graft System

Treatment groups

100 Participants
are divided into 1 treatment group

Sponsors and collaborators