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Cleaner Long-tErm Assessment Registry - Venous Insights and Efficacy With eXtended Tracking
NCT07102160 · View on ClinicalTrials.gov ↗
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 Studied
Interventions
- DEVICE Aspiration thrombectomy system
Study Locations (3)
Florida
- Baycare Health System — Tampa
Kentucky
- St. Elizabeth Healthcare - Edgewood — Edgewood
Texas
- Baylor Scott & White The Heart Hospital - Plano — Plano
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 185 participants |
| Start Date | 2026-02-04 |
| Est. Completion | 2029-06 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07102160
The ClinicalTrials.gov registry entry for NCT07102160 describes a study currently listed as recruiting. It is categorized as an unspecified phase, 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 185 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Argon Medical Devices, which has 2 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 4 conditions, with Deep Vein Thrombosis (DVT) appearing as the primary indexed condition, and to 1 intervention — of which Aspiration 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: NCT07102160 reports 3 study locations spanning 3 distinct geographic areas — top geographies include Florida, Kentucky, Texas. 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 NCT07102160 about?
NCT07102160 is a clinical study titled "Cleaner Long-tErm Assessment Registry - Venous Insights and Efficacy With eXtended Tracking". 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 cl...
What is the current status of trial NCT07102160?
This trial is currently recruiting. The enrollment target is 185 participants. The study started on 2026-02-04. Estimated completion is 2029-06.
What conditions does trial NCT07102160 study?
This clinical trial studies the following conditions: Deep Vein Thrombosis (DVT), Venous Embolism, Thrombus in the Peripheral Venous Vasculature, Thrombus in the Central and Peripheral Circulatory System, Including Saphenous Vein Grafts. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT07102160?
The interventions under investigation include: Aspiration thrombectomy system (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT07102160?
This trial is sponsored by Argon Medical Devices, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT07102160 being conducted?
This trial has 3 study locations across Florida, Kentucky, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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