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Cleaner Long-tErm Assessment Registry - Venous Insights and Efficacy With eXtended Tracking

NCT07102160 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 185

Last updated 2026-05-01

No results posted yet for this study

Summary

The primary objective of this clinical investigation is to evaluate the safety and effectiveness of the Cleaner Vac® Thrombectomy System for the treatment of thrombus in patients with lower extremity proximal deep vein thrombosis (DVT). This prospective, multi-center, open-label study will assess clinical outcomes, device performance, and procedural success in a single DVT study cohort.

Conditions

  • Deep Vein Thrombosis (DVT)
  • Thrombus in the Peripheral Venous Vasculature
  • Venous Embolism
  • Thrombus in the Central and Peripheral Circulatory System, Including Saphenous Vein Grafts

Interventions

DEVICE

Aspiration thrombectomy system

The Cleaner Vac® Thrombectomy System is a percutaneous mechanical aspiration thrombectomy device designed for the removal of fresh, soft thrombi and emboli from the peripheral venous vasculature. The system includes an aspiration canister with integrated pump, an 18F aspiration catheter, a handpiece with aspiration control lever, a dilator, and an optional flushing adapter. The device operates via controlled suction to extract thrombus and restore venous patency.

Sponsors & Collaborators

  • Avania

    collaborator INDUSTRY

  • Medical Metrics Diagnostics, Inc

    collaborator INDUSTRY

  • Argon Medical Devices

    lead INDUSTRY

Principal Investigators

  • Pete Stibbs · Argon Medical Devices

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-02-04
Primary Completion
2029-06-30
Completion
2029-06-30
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07102160 on ClinicalTrials.gov