In this double-blind, placebo-controlled week trial, the anxiolytic properties of the nonbenzodiazepine buspirone were compared with the benzodiazepine lorazepam and placebo in "buspar and lorazepam together" with generalized anxiety disorder according to DSM-III. The study also comprised a 2-week taper period and a 4-week placebo-control period to assess the stability of clinical improvement.

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