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Decellularized Femoral Artery Allograft (Nexeon AVX) Prospective Registry

End-Stage Renal Disease Clinical Trial

Official title:
Safety, Efficacy, & Use of Decellularized Femoral Artery Allograft for Arteriovenous Access for Hemodialysis: A Multi-center Prospective Registry Study

Clinical Trial Summary

Post market registry to assess the safety and efficacy of a novel decellularized human femoral artery allograft (Nexeon AVX Decellularized Femoral Artery,

Clinical Trial Description

The clinical objective of this prospective, observational, post market registry study, CR-21-005, is to assess the safety and efficacy of a decellularized human femoral artery allograft (Nexeon AVX Decellularized Femoral Artery, LifeNet Health, Virginia Beach, VA) in the creation of vascular access for hemodialysis in patients with ESRD. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05880537
Study type Observational [Patient Registry]
Source LifeNet Health
Contact Kimberly Dorsch
Phone 757-609-4378
Email kimberly_dorsch@lifenethealth.org
Status Recruiting
Phase
Start date June 6, 2023
Completion date December 15, 2027
View Details
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