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Clinical Trial Summary

Multi-center trial to assess the feasibility and safety of the EchoMark LP and the EchoMark diagnostic ultrasound system for assessing AV fistula blood flow, diameter, and depth.


Clinical Trial Description

This is a prospective, multi-center, single-arm, non-blinded clinical trial designed to evaluate the feasibility and safety of the EchoMark and the EchoSure in subjects undergoing new upper arm autologous arteriovenous fistula creation who require hemodialysis. All subjects will provide informed consent prior to undergoing any study procedures. The study will consists of multiple follow-up visits during the 52 week duration. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04896476
Study type Interventional
Source Sonavex, Inc.
Contact
Status Active, not recruiting
Phase N/A
Start date January 21, 2022
Completion date June 6, 2025

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