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Clinical Trial Summary

Prospective, single-center study to evaluate the everlinQ endoAVF System when used to create an endoAVF in hemodialysis patients. This study aims to investigate expansion of the percutaneous venous access location to the superficial system which may provide additional procedural benefit.


Clinical Trial Description

A total of up to 50 subjects will be enrolled and will undergo an endoAVF creation procedure using the everlinQ System. All subjects may be followed for up to 12 months post index procedure based on Investigator's discretion. The duration of the study is expected to be approximately two (2) years. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03708562
Study type Interventional
Source TVA Medical Inc.
Contact
Status Completed
Phase N/A
Start date October 16, 2017
Completion date December 12, 2018

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