Stroke, Vol 23, 519-526, Copyright © 1992 by American Heart Association
WA Rocca, FC Dorsey, F Grigoletto, M Gent, RS Roberts, MD Walker, JD Easton, R Bruno, A Carolei and G Sancesario
BACKGROUND AND PURPOSE: The Early Stroke Trial is a randomized, placebo-
controlled, double-masked, multicenter study to assess the safety and
efficacy of monosialoganglioside in patients who have suffered an ischemic
stroke of the cerebral hemispheres. METHODS: Only patients who could be
evaluated and treated within 5 hours after the onset of stroke were
considered; within each center, subjects were stratified by age, sex, and
clinical severity. Patients were randomly allocated to receive a specified
sequence of intravenous and intramuscular doses of either
monosialoganglioside or identical-appearing placebo for 21 days. Patients
were followed up for 4 months after randomization. Neurological status was
measured primarily by using the Canadian Neurological Scale. After
assessing the effect of treatment on survival, the principal measure of
efficacy will be the change in neurological status between baseline and the
4-month follow-up among survivors. RESULTS: Sixteen clinical centers, 15 in
Europe and one in North America, entered a total of 792 eligible patients
during a 36- month recruitment period (from May 1987 to April 1990). In our
series there were more men than women, and the relative frequency of
patients increased with advancing age. The most frequently associated
cardiovascular conditions were hypertension, atrial fibrillation, and
peripheral vascular disease. Approximately 46% of the patients were
admitted to a hospital within 1 hour and 81%, within 2 hours after the
onset of stroke. About 22% first received the study treatment within 3
hours and 57%, within 4 hours. CONCLUSIONS: This study demonstrates the
feasibility of large-scale trials with the onset of treatment within 5
hours after an ischemic stroke.
ARTICLES
Design and baseline results of the monosialoganglioside early stroke trial. The EST Study Group
Epidemiology and Clinical Research, Verona, Italy.
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