Stroke, Vol 20, 1143-1149, Copyright © 1989 by American Heart Association
C Argentino, ML Sacchetti, D Toni, G Savoini, E D'Arcangelo, F Erminio, F Federico, FF Milone, V Gallai and D Gambi
Eleven of 31 clinical centers participating in the Italian Acute Stroke
Study--Hemodilution carried out a preliminary study on the effectiveness of
ganglioside GM1 in acute stroke; 502 patients were randomized to GM1 (GM1,
n = 121), GM1 plus hemodilution (GM1 + H, n = 128), placebo (P, n = 130),
or placebo plus hemodilution (P + H, n = 123) groups less than or equal to
12 hours after onset of a hemispheric cerebral infarct. The patients were
treated for 15 days and were evaluated on Days 21 and 120 after the onset
of stroke. Intention-to- treat analysis failed to show any differences in
neurologic deficit, mortality, or neurologic disability among the groups.
Efficacy analysis showed a significantly higher degree of neurologic
improvement in GM1 group patients compared with patients in the P group
during the first 15 days. GM1-treated patients (GM1 and GM1 + H groups)
showed a significantly higher degree of neurologic improvement during the
first 10 days compared with the placebo-treated patients (P and P + H
groups). These differences were no longer statistically significant at Day
120. Our results provide a rationale for the planning of a larger,
multicenter trial of GM1 ganglioside in acute stroke.
ARTICLES
GM1 ganglioside therapy in acute ischemic stroke. Italian Acute Stroke Study--Hemodilution + Drug
Dipartimento di Scienze Neurologiche, Roma, Italy.
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