This is a multicenter, randomized, double-blind, placebo-controlled clinical trial.
The aim i s to evaluate the effect of Lubeluzole compared to placebo in the treatment of acute ischemic stroke within 8 hours. The primary hypothesis is that the lubeluzole will reduce mortality without increasing morbidity, therefore the primary endpoint is mortality at 12 weeks and the seconday end-points are functional and neurological recovery.
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