🏛️ Verified NIH Record • Updated 2025-08-12

Early Feasibility Study of the Velocity™ Percutaneous Arterio-Venous Fistula System for Creating Hemodialysis Vascular Access (NCT06712251)

Early Feasibility Study of the Velocity™ Percutaneous Arterio-Venous Fistula System

🔵 Active, Not Recruiting Observational / Diagnostic ⚙️ Medical Device Protocol Sponsor: Venova Medical

🩺 Plain-English Summary (8th-Grade Level)

The Velocity Percutaneous Arterio-Venous System is a minimally invasive method of creating hemodialysis vascular access. The study aims to understand clinical efficacy and initial clinical safety data of the device.

Who can join: Review the eligibility criteria below.

Location: Trinity Research Group — Dothan, Alabama

Age range: 18 Years to 80 Years

🧪 Interventions in This Study

📋 "Do I Qualify?" — 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria ↗

📍 All Participating Trial Locations (5 Sites)

  • Trinity Research Group — Dothan, Alabama
  • Apex Research — Riverside, California
  • American Access Care of Jacksonville — Jacksonville, Florida
  • Texas Research Institute — Fort Worth, Texas
  • STAR Vascular — San Antonio, Texas

💰 Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

More studies in Chronic Kidney Disease Requiring Hemodialysis

💡 How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Review the official NIH record below to find the coordinating site.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
🏛️ View Official NIH Record ↗