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Clinical Trial Summary

This study will assess the safety and efficacy of a completely autologous and completely biological tissue engineered blood vessel (TEBV) called Lifelineā„¢ used as an arteriovenous fistula for dialysis access.


Clinical Trial Description

n/a


Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00850252
Study type Interventional
Source Cytograft Tissue Engineering
Contact
Status Completed
Phase Phase 1/Phase 2
Start date September 2004
Completion date December 2012

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