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RECRUITING NA

FastWire REvascularisation of Extremities, (For LOWer Limbs) - FREEFLOW

NCT06492733 · View on ClinicalTrials.gov ↗

Study Summary

This study is to assess the safety and efficacy of the FastWire System. It is intended to assess that the FastWire System can facilitate the intra-luminal placement of conventional guidewires or treatment devices beyond peripheral artery chronic total occlusions (CTOs)

Interventions

  • DEVICE FastWire System - Peripheral

Study Locations (6)

Delaware

  • EndoVascular Consultants — Wilmington

Florida

  • Vascular & Embolization Specialists — Cocoa

Iowa

  • Vascular Institute of the Midwest — Davenport

Louisiana

  • Cardiovascular Institute of the South-ASC — Gray

Michigan

  • Dearborn Cardiology — Dearborn

Tennessee

  • Vascular Institute of Chattanooga — Chattanooga

Trial Details

FieldValue
Enrollment Target 65 participants
Start Date 2024-11-05
Est. Completion 2026-07
Phase NA

Sponsor

Versono Medical

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06492733

The ClinicalTrials.gov registry entry for NCT06492733 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 65 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Versono Medical, 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 1 condition, with Chronic Total Occlusion of Artery of the Extremities appearing as the primary indexed condition, and to 1 intervention — of which FastWire System - Peripheral 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: NCT06492733 reports 6 study locations spanning 6 distinct geographic areas — top geographies include Delaware, Florida, Iowa. 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 NCT06492733 about?

NCT06492733 is a clinical study titled "FastWire REvascularisation of Extremities, (For LOWer Limbs) - FREEFLOW". This study is to assess the safety and efficacy of the FastWire System. It is intended to assess that the FastWire System can facilitate the intra-luminal placement of conventional guidewires or treatment devices beyond peripheral artery chronic total occlusions (CTOs)

What is the current status of trial NCT06492733?

This trial is currently recruiting. It is a NA study. The enrollment target is 65 participants. The study started on 2024-11-05. Estimated completion is 2026-07.

What conditions does trial NCT06492733 study?

This clinical trial studies the following conditions: Chronic Total Occlusion of Artery of the Extremities. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06492733?

The interventions under investigation include: FastWire System - Peripheral (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06492733?

This trial is sponsored by Versono Medical, 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 NCT06492733 being conducted?

This trial has 6 study locations across Delaware, Florida, Iowa, Louisiana, Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial