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NCT06189313 · ClinicalTrials.gov registry record · NA
CLEANer Aspiration for Pulmonary Embolism
A NA study of Cardiovascular Diseases and Pulmonary Embolism, sponsored by Argon Medical Devices.
- Recruiting
- Registry status
- NA
- Development phase
- 125
- Enrollment target
- 14
- Study locations
NCT06189313 is a NA study of Cardiovascular Diseases and Pulmonary Embolism that is actively recruiting participants, run by Argon Medical Devices. The registered enrollment target is 125 participants, below the 26,974-participant average among 300 other Cardiovascular Diseases trials with a reported enrollment target (100% lower). The trial reports 14 study locations across 10 states.
The verdict
NCT06189313, a NA study of Cardiovascular Diseases and Pulmonary Embolism, is actively recruiting participants, sponsored by Argon Medical Devices.
- RECRUITING
- Registry status
- NA
- Development phase
- 125 participants
- Enrollment target
- 14
- Study locations
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 |
Interested in This Trial?
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, categorized as NA. The registered enrollment target is 125 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 26,974-participant average among 300 other Cardiovascular Diseases trials with a reported enrollment target (100% lower). The listed sponsor is Argon Medical Devices, which has 4 total studies on file at ClinicalTrials.gov.
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.
NCT06189313 reports 14 study locations spanning 10 distinct geographic areas - top geographies include Ohio, Florida, Texas.
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.
What interventions are being tested in trial NCT06189313?
The interventions under investigation include: Cleaner Pro Thrombectomy System (DEVICE).
Who is sponsoring clinical trial NCT06189313?
This trial is sponsored by Argon Medical Devices, which has 4 total clinical trials registered on ClinicalTrials.gov.
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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