Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING NA

The ArtixASCEND Study

NCT07135895 · View on ClinicalTrials.gov ↗

Study Summary

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.

Interventions

  • DEVICE Artix Thrombectomy System

Study Locations (5)

Connecticut

  • Yale University — New Haven

District of Columbia

  • MedStar Washington Hospital Center — Washington D.C.

North Carolina

  • Mission Memorial Hospital — Asheville

Oklahoma

  • Ascension St. John Jane Phillips Medical Center — Bartlesville

South Carolina

  • Grand Strand Medical Center — Myrtle Beach

Trial Details

FieldValue
Enrollment Target 250 participants
Start Date 2026-01-07
Est. Completion 2029-10-01
Phase NA

Sponsor

Inari Medical

5 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07135895

The ClinicalTrials.gov registry entry for NCT07135895 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 250 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Inari Medical, which has 5 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Acute Lower Limb Arterial Occlusion appearing as the primary indexed condition, and to 1 intervention — of which Artix Thrombectomy System is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT07135895 reports 5 study locations spanning 5 distinct geographic areas — top geographies include Connecticut, District of Columbia, North Carolina. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT07135895 about?

NCT07135895 is a clinical study titled "The ArtixASCEND Study". 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.

What is the current status of trial NCT07135895?

This trial is currently recruiting. It is a NA study. The enrollment target is 250 participants. The study started on 2026-01-07. Estimated completion is 2029-10-01.

What conditions does trial NCT07135895 study?

This clinical trial studies the following conditions: Acute Lower Limb Arterial Occlusion. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT07135895?

The interventions under investigation include: Artix Thrombectomy System (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT07135895?

This trial is sponsored by Inari Medical, which has 5 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT07135895 being conducted?

This trial has 5 study locations across Connecticut, District of Columbia, North Carolina, Oklahoma, South Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial