Pilot Study of Clinical Safety and Feasibility of the Neuro-Spinal ScaffoldTM for the Treatment of Complete (AIS A) Traumatic Acute Spinal Cord Injury at the C5-T1 Neurological Levels The purpose of this study is to support an expansion to support marketing applications as well as future studies.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
DEVICE_FEASIBILITY
Masking
NONE
Experimental: Neuro-Spinal Scaffold
Toronto Western Hospital
Toronto, Ontario, Canada
Incidence of all Adverse Device Effects of any kind/seriousness.
Time frame: 6 Months
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