Abstract
Background: Well-tolerated and effective therapies for bipolar mania are required. Aims: To evaluate the efficacy and tolerability of aripiprazole as acute and maintenance of effect therapy in patients with bipolar I disorder experiencing manic or mixed episodes. Method: Patients were randomised to double-blind aripiprazole (15 or 30 mg/day; n=167), placebo (n=153) or haloperidol (5-15 mg/day, n=165) for 3 weeks (trial registration NCT00097266). Aripiprazole- and haloperidol-treated patients remained on masked treatment for 9 additional weeks. Results: Mean change in Young Mania Rating Scale Total score (primary end-point) at week 3 was significantly greater with aripiprazole (-12.0; P < 0.05) and haloperidol (-12.8; P < 0.01) than with placebo (-9.7). Improvements were maintained to week 12 for aripiprazole (-17.2) and haloperidol (-17.8). Aripiprazole was well tolerated. Extrapyramidal adverse events were more frequent with haloperidol than aripiprazole (53.3% v. 23.5%). Conclusions: Clinical improvements with aripiprazole were sustained to week 12. Aripiprazole was generally well tolerated.
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CITATION STYLE
Young, A. H., Oren, D. A., Lowy, A., McQuade, R. D., Marcus, R. N., Carson, W. H., … Sanchez, R. (2009). Aripiprazole monotherapy in acute mania: 12-Week randomised placebo- and haloperidol-controlled study. British Journal of Psychiatry, 194(1), 40–48. https://doi.org/10.1192/bjp.bp.108.049965
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