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Active Not RecruitingNCT06712251

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

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

Status
Active Not Recruiting
Phase
N/A
Study type
Interventional
Enrollment
20 (estimated)
Sponsor
Venova Medical · Industry
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
DEVICEVelocity pAVF SystemThe Velocity Percutaneous Arterio-Venous Fistula System consists of a percutaneous method designed to create an arteriovenous fistula for hemodialysis vascular access.

Timeline

Start date
2025-01-08
Primary completion
2025-05-15
Completion
2027-01-04
First posted
2024-12-02
Last updated
2025-08-17

Locations

5 sites across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT06712251. Inclusion in this directory is not an endorsement.

Early Feasibility Study of the Velocity™ Percutaneous Arterio-Venous Fistula System for Creating Hemodialysis Vascular A (NCT06712251) · Clinical Trials Directory