Inclusion criteria |
Age ≥18 and ≤70 years |
Written informed consent by patient or legally authorized representative to participate in the study |
No other life-threatening injury |
Nonpenetrating spinal cord injury at neurologic level from C4 to T11 |
ASIA Impairment Scale grade A, B, or C |
No cognitive impairment that would preclude an informed consent, including moderate or severe traumatic brain injury |
Initial dose of riluzole within 12 h of injury |
Exclusion criteria |
Hypersensitivity to riluzole or any of its components |
Unable to receive riluzole orally or by nasogastric tube |
History of liver or kidney disease (e.g., hepatitis A, B, or C or cirrhosis) |
A recent history of regular substance abuse (illicit drugs or alcohol) |
Unconscious |
Penetrating spinal cord injury |
Pregnancy as established by urine pregnancy test |
Currently involved in another spinal cord injury research study |
Has a mental disorder or other illness, which, in the view of the site investigator, would preclude accurate medical and neurological evaluation |
Unable to commit to the follow-up schedule |
Is a prisoner |
Unable to converse, read, and write in English at the elementary-school level |