The purpose of this investigation was to study the effectiveness of ga
bapentin in controlling spasticity in persons with spinal cord injury
(SCI) using a surface EMG-based quantitative assessment technique call
ed the brain motor control assessment (BMCA). Six men from a Veterans
Affairs Medical Center with spasticity due to traumatic SCI were studi
ed as part of a multi-center, placebo-controlled, cross-over, clinical
trial of gabapentin. Spasticity was evaluated using multi-channel sur
face EMG recordings of muscles in the lower extremities, abdomen and l
ow back before and during treatment with oral gabapentin or placebo. G
abapentin or placebo was given orally in doses 400 mg three times dail
y for 48 h. Following a 10 day wash-out period subjects were crossed-o
ver to receive the medication not received the first time. This was fo
llowed by an elective open-label extension. Group results during the c
ontrolled trial did not reach statistical significance at the dosage u
sed. One subject demonstrated a dramatic improvement in spasticity tha
t was apparent both clinically and with the BMCA. Other subjects demon
strated modest improvements which were seen in the BMCA but not recogn
ized clinically. During the open label extension, the four subjects wh
o participated experienced important clinical improvements with higher
doses (to 3600 mg/day). These improvements were often in components o
f spasticity in which the BMCA had detected subclinical changes during
the cross-over trial. A seventh subject was studied using the BMCA at
doses of 1200 mg T.I.D. gabapentin, off gabapentin and 800 mg T.I.D.
gabapentin and demonstrated quantitatively a dose-related effect with
higher doses of gabapentin which matched clinical observations. Gabape
ntin at doses of 400 mg T.I.D. may be effective in controlling some fe
atures of spasticity in persons with SCI. Higher doses provide greater
control of spasticity, and controlled studies using higher doses are
needed to evaluate gabapentin's efficacy.