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ABSTRACT: Introduction
Acute traumatic spinal cord injury (tSCI) is a devastating neurological disorder with no pharmacological neuroprotective strategy proven effective to date. Progressive haemorrhagic necrosis (PHN) represents an increasingly well-characterised mechanism of secondary injury after tSCI that negatively impacts neurological outcomes following acute tSCI. Preclinical studies evaluating the use of the Food and Drug Administration-approved sulfonylurea receptor 1-transient receptor potential melastatin 4 channel blocker glyburide in rodent models have shown reduced secondary microhaemorrhage formation and the absence of capillary fragmentation, the pathological hallmark of PHN.Methods and analysis
In this initial phase multicentre open-label pilot study, we propose to e
SUBMITTER: Minnema AJ
PROVIDER: S-EPMC6797422 | biostudies-literature | 2019 Oct
REPOSITORIES: biostudies-literature