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CLEANer Aspiration for Pulmonary Embolism
NCT06189313 · View on ClinicalTrials.gov ↗
Study Summary
To evaluate the safety and efficacy of the Cleaner™ Pro Thrombectomy System for aspiration thrombectomy in patients with acute pulmonary embolism (PE).
Conditions Studied
Interventions
- DEVICE Cleaner Pro Thrombectomy System
Study Locations (14)
Ohio
- University of Cincinnati — Cincinnati
- Cleveland Clinic — Cleveland
- Promedica Toledo Hospital — Toledo
Florida
- Ascension Sacred Heart Hospital — Pensacola
- BayCare Health System — Tampa
Texas
- Baylor Scott and White Heart and Vascular Hospital - Dallas — Dallas
- Baylor Scott & White The Heart Hospital - Plano — Plano
Colorado
- University of Colorado Anschutz Medical Campus — Aurora
District of Columbia
- Medstar Health Research Institute — Washington D.C.
Illinois
- Insight Hospital and Medical Center — Chicago
Indiana
- Ascension St. Vincent Hospital — Indianapolis
Massachusetts
- UMass Chan Medical School — Worcester
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 125 participants |
| Start Date | 2025-01-03 |
| Est. Completion | 2027-09-02 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06189313
The ClinicalTrials.gov registry entry for NCT06189313 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 125 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 Cardiovascular Diseases appearing as the primary indexed condition, and to 1 intervention — of which Cleaner Pro 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: NCT06189313 reports 14 study locations spanning 10 distinct geographic areas — top geographies include Ohio, Florida, 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 NCT06189313 about?
NCT06189313 is a clinical study titled "CLEANer Aspiration for Pulmonary Embolism". To evaluate the safety and efficacy of the Cleaner™ Pro Thrombectomy System for aspiration thrombectomy in patients with acute pulmonary embolism (PE).
What is the current status of trial NCT06189313?
This trial is currently recruiting. It is a NA study. The enrollment target is 125 participants. The study started on 2025-01-03. Estimated completion is 2027-09-02.
What conditions does trial NCT06189313 study?
This clinical trial studies the following conditions: Cardiovascular Diseases, Pulmonary Embolism, Venous Thromboembolism, Acute Pulmonary Embolism. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06189313?
The interventions under investigation include: Cleaner Pro Thrombectomy System (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06189313?
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 NCT06189313 being conducted?
This trial has 14 study locations across Colorado, District of Columbia, Florida, Illinois, Indiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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