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Clinical Trial Summary

Feasibility of the Vessel Restoration System for AVF


Clinical Trial Description

A study of the safety and feasibility of the Vessel Restoration System for AVF to promote the physiologic and functional maturation of a Brachiocephalic End-to-Side Arteriovenous Fistulas (AVF) in Patients with Chronic Kidney Disease Stage V (Pre-dialysis): ACTIVATE AVF ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05462223
Study type Interventional
Source Alucent Biomedical
Contact Kate Ecklund, MPH
Phone 3857722300
Email kecklund@alucentbiomedical.com
Status Recruiting
Phase N/A
Start date July 15, 2022
Completion date December 15, 2024

See also
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Completed NCT01471041 - Safety and Efficacy Study of the Venous Window Needle Guide to Access Arteriovenous (AV)Fistulae Phase 2/Phase 3
Not yet recruiting NCT05569109 - av Fistula Patency Loss as a Cause of Fistula Failure and Hyperphosphatemia
Completed NCT02475837 - Vorapaxar Study for Maturation of AV Fistulae for Hemodialysis Access Phase 2
Active, not recruiting NCT04484220 - Ellipsys Vascular Access System Post Market Surveillance (PS) Study N/A
Active, not recruiting NCT04327609 - SAVE Trial - Use of the Selution Sirolimus Eluting Balloon for Dysfunctional AV accEss Treatment Indications N/A