Nexeon Arterial Venous Allograft
OtherNexeon AVX allograft for hemodialysis access in end stage renal disease
NCT Number: NCT05880537
Post market registry to assess the safety and efficacy of a novel decellularized human femoral artery allograft (Nexeon AVX Decellularized Femoral Artery,
Interested in participating?
Request Info18 year and older
All sexes
Observational
Infirmary Heath, Mobile, Alabama, United States
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Nexeon AVX allograft for hemodialysis access in end stage renal disease
Time frame: 24 months
Ultrasound proof of vessel patency and blood flow
Time frame: 24 months
Evaluating the emergent adverse events as it pertains to the hemodialysis access anatomical site
Contact information is provided by the study sponsor or research team.
Kimberly Dorsch
CONTACT
Monique Alston-Epps
CONTACT
LifeNet Health
Industry
Safety, Efficacy, & Use of Decellularized Femoral Artery Allograft for Arteriovenous Access for Hemodialysis: A Multi-center Prospective Registry Study
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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