The ArtixASCEND Study

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorInari Medical

About this trial

This study is a post-market, prospective, multicenter, single-arm study to evaluate the safety and effectiveness of the Artix Thrombectomy System in patients with acute lower extremity arterial occlusions.

Eligibility criteria

Qualifiers

Age ≥ 18 years

Acute symptom duration ≤ 14 days

Lower limb arterial occlusion below inguinal ligament

Target lesion in native vessel

Disqualifiers

Life expectancy < 6 months

Prior major amputation in the target limb

Prior minor amputation in the target limb that is not completely healed or cannot bear weight

Non-thrombotic occlusion secondary to dissection, vasculitis, or target vessel trauma

Trial design

Treatments tested in this trial

  • Artix Thrombectomy System

Treatment groups

250 Participants
are divided into 1 treatment group

Sponsors and collaborators