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Automated 3D Ultrasound-based Surveillance of Arteriovenous Fistula Maturation for Post-operative Hemodialysis Patients

Arteriovenous Fistula Clinical Trial

Official title:
Automated 3D Ultrasound-based Surveillance of Arteriovenous Fistula Maturation for Post-operative Hemodialysis Patients

Clinical Trial Summary

This is a two stage, prospective, multi-center study to evaluate the EchoMark and EchoSure devices in patients undergoing peripheral arteriovenous fistula creation for hemodialysis access.

Clinical Trial Description

This is Stage 1 of a 2 stage protocol, targeting to enroll 60 patients in prospective, single arm, non-randomized, multi-center observational study to record objective data in patients undergoing upper extremity arteriovenous fistula construction with autologous tissue for the purpose of eventual hemodialysis access, in whom the EchoMark is placed at the site of vascular anastomosis. Follow-up visits include EchoSure and duplex imaging. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04017910
Study type Observational
Source Sonavex, Inc.
Contact
Status Terminated
Phase
Start date December 2, 2019
Completion date May 12, 2021
View Details
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