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Evaluation of a Simple-Prep Controlled Embolic
NCT06453642 · View on ClinicalTrials.gov ↗
Study Summary
The objective of this study is to evaluate the safety and effectiveness of the GPX® Embolic Device when used as indicated for embolization requiring distal vessel penetration in 114 subjects in up to 25 investigational sites in the USA, New Zealand, and Canada.
Conditions Studied
Interventions
- DEVICE GPX® Embolic Device
Study Locations (20)
New York
- Albany Medical Center — Albany
- Mount Sinai — New York
- Memorial Sloan Kettering Cancer Center — New York
Ontario
- St. Michael's Hospital — Toronto
- Toronto General Hosptial — Toronto
- Mount Sinai Hospital Toronto — Toronto
North Carolina
- University of North Carolina — Chapel Hill
- Atrium Health Carolinas Medical Center — Charlotte
Texas
- University of Texas Southwestern — Dallas
- MD Anderson Cancer Center - Interventional Radiology — Houston
Other
- Auckland City Hospital — Auckland
- Christchurch Hospital — Christchurch
California
- University of California San Diego Altman Clinical and Translation Research Institute — La Jolla
Colorado
- University of Colorado Anschutz Medical Campus — Aurora
Illinois
- Northwestern University — Chicago
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 114 participants |
| Start Date | 2024-11-18 |
| Est. Completion | 2026-09 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06453642
The ClinicalTrials.gov registry entry for NCT06453642 describes a study currently listed as active not 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 114 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Fluidx Medical Technology, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 6 conditions, with Renal Cell Carcinoma appearing as the primary indexed condition, and to 1 intervention — of which GPX® Embolic Device 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: NCT06453642 reports 20 study locations spanning 13 distinct geographic areas — top geographies include New York, Ontario, 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 NCT06453642 about?
NCT06453642 is a clinical study titled "Evaluation of a Simple-Prep Controlled Embolic". The objective of this study is to evaluate the safety and effectiveness of the GPX® Embolic Device when used as indicated for embolization requiring distal vessel penetration in 114 subjects in up to 25 investigational sites in the USA, New Zealand, and Canada.
What is the current status of trial NCT06453642?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 114 participants. The study started on 2024-11-18. Estimated completion is 2026-09.
What conditions does trial NCT06453642 study?
This clinical trial studies the following conditions: Renal Cell Carcinoma, Bone Tumor, Embolization, Vascular Tumor, Renal Angiomyolipoma. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06453642?
The interventions under investigation include: GPX® Embolic Device (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06453642?
This trial is sponsored by Fluidx Medical Technology, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06453642 being conducted?
This trial has 20 study locations across California, Colorado, Illinois, Indiana, Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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