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- W2075316624 abstract "The purpose of the present study was to evaluate zuclopenthixol acetate in Viscoleo®, a new preparation to be administered once every 3 days, in the early treatment of acute psychotic episodes and acute deterioration of chronic psychosis. 21 cases were included in the study: patients received 1 to 3 injections. Clinical evaluation was made at 24, 48 and 72 hours after each injection, using the Clinical Global Impressions (CGI) and the Brief Psychiatric Rating Scale (BPRS). Results at end-point indicated a marked or moderate therapeutic effect in the 11 cases of acute psychosis. A statistically significant decrease was observed for the total BPRS score as well as for its subscales. Among 8 cases of exacerbation of chronic psychosis, 4 patients showed a moderate therapeutic effect, and minimal or no effect was found in the other 4 subjects. The total BPRS decreased significantly, but to a lesser extent than for acute psychosis. Two patients suffering from mania showed a moderate therapeutic effect according to CGI. 8 cases of acute psychosis and 5 cases of chronic psychosis did not suffer from any neurological side-effects. Plasma concentration measurements suggest that a dose of 50 mg per 3 days may be sufficient for early treatment of most acutely ill psychotic patients." @default.
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- W2075316624 date "1989-11-01" @default.
- W2075316624 modified "2023-09-23" @default.
- W2075316624 title "Clinical and Pharmacokinetic Evaluation of Zuclopenthixol Acetate in Viscoleo®" @default.
- W2075316624 doi "https://doi.org/10.1055/s-2007-1014609" @default.
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