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Stein D.J. Khoo J.P. Van Ameringen D.M. Hoschl C., Ahokas A., Bauer M., Bitter I., Jarema M., Mosolov S., Vavrusova L., Picarel-Blanchot F., Matharan S., Olivier V.
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European Neuropsychopharmacology
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AIM OF THE ANALYSIS
The present analysis assesses the 12-week efficacy and safety of agomelatine 25-50 mg versus escitalopram 10-20 mg in non-depressed outpatients with severe generalized anxiety disorder (GAD).
METHOdS
In this phase III, multicenter, international, randomized, double-blind, comparative trial, 523 patients were randomized into two parallel groups: agomelatine 25-50 mg (n=261) or escitalopram 10-20 mg (n=262).
RESULTS
Randomized patients had a mean age of 41 years, and 69% of them were female. All patients fulfilled DSM-IV diagnostic criteria for GAD and experienced functional impairment according to the Sheehan Disability Scale (SDS).
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