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A placebo-controlled, random-assignment, parallel-group pilot study of adjunctive topiramate for patients with schizoaffective disorder, bipolar type.

A placebo-controlled, random-assignment, parallel-group pilot study of adjunctive topiramate for patients with schizoaffective disorder, bipolar type. Research Abstract Details 

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  • A placebo-controlled, random-assignment, parallel-group pilot study of adjunctive topiramate for patients with schizoaffective disorder, bipolar type. Abstract Text:

    kn roy chengappaKn Roy Chengappa,david j kupferDavid J Kupfer,haranath parepallyHaranath Parepally,vineeth johnVineeth John,ranita basuRanita Basu,joan buttenfieldJoan Buttenfield,patricia schlichtPatricia Schlicht,patricia houckPatricia Houck,jaspreet s brarJaspreet S Brar,samuel gershonSamuel Gershon,kn roy chengappaKn Roy Chengappa,david j kupferDavid J Kupfer,haranath parepallyHaranath Parepally,vineeth johnVineeth John,ranita basuRanita Basu,joan buttenfieldJoan Buttenfield,patricia schlichtPatricia Schlicht,patricia houckPatricia Houck,jaspreet s brarJaspreet S Brar,samuel gershonSamuel Gershon,

    OBJECTIVES: This pilot study evaluated the efficacy and safety of adjunctive topiramate compared with placebo in the treatment of patients with a diagnosis of schizoaffective disorder, bipolar type (SAD-BT). METHODS: A sample of 48 adult patients with a Diagnostic and Statistical Manual of Mental Disorders, 4th Edition, Text Revision (DSM-IV-TR) diagnosis of SAD-BT (supported by the Structured Clinical Interview for DSM-IV Axis I Disorder, Patient Edition) were randomly assigned in a 2:1 ratio (favoring topiramate) to 8 weeks of double-blind treatment with topiramate (100-400 mg/day) or placebo. Patients who had achieved a > or =20% decrease from baseline in their Positive and Negative Syndrome Scale (PANSS) total scores were given the opportunity to continue for an additional 8 weeks of double-blind treatment. The dosage of the study medicine was continued unchanged from the earlier 8-week study period. At the end of the study period, the study medicine was tapered and discontinued over a 2-week period. Primary efficacy was assessed at 8 weeks using the mean change between treatment groups of the PANSS total scores in the intent-to-treat population of randomized patients. Several secondary measures were also assessed. Safety analyses included monitoring of adverse events, vital signs, electrocardiogram (ECG) and laboratory values. RESULTS: Even though both treatments reduced scores on various psychopathology rating scales, adjunctive topiramate treatment (nearly 275 mg/day) did not show increased efficacy relative to placebo on the primary outcome measure (PANSS scale) or any of the secondary outcome measures. Topiramate-treated patients lost significantly more body weight than placebo-treated patients, which led to a significant reduction in body mass index (BMI). Relative to adjunctive placebo, topiramate-treated patients experienced higher rates of paresthesia, sedation, word-finding difficulty, sleepiness, and forgetfulness, but these differences were not statistically significant. There were no clinically significant abnormalities in either the ECG or laboratory results. There were no serious adverse events in the study. Further, there was no worsening of the PANSS total scores (to > or =10% from baseline), and no significant differences between the treatments on worsening of total Montgomery-Asberg Depression Rating Scale (MADRS) scores [1/13 (7.7%) for placebo; 1/25 (4.0%) for topiramate]. CONCLUSIONS: This pilot study did not support clinical efficacy for adjunctive topiramate treatment in patients with SAD-BT. There were no major safety or tolerability issues in this study. Confirming the results of other studies, topiramate-treated patients did experience greater body weight loss and reduction in BMI.

    A placebo-controlled, random-assignment, parallel-group pilot study of adjunctive topiramate for patients with schizoaffective disorder, bipolar type. Publishing Authors By Initials

    k roy chengappaK Roy Chengappa,dj kupferDJ Kupfer,h parepallyH Parepally,v johnV John,r basuR Basu,j buttenfieldJ Buttenfield,p schlichtP Schlicht,p houckP Houck,js brarJS Brar,s gershonS Gershon,k roy chengappaK Roy Chengappa,dj kupferDJ Kupfer,h parepallyH Parepally,v johnV John,r basuR Basu,j buttenfieldJ Buttenfield,p schlichtP Schlicht,p houckP Houck,js brarJS Brar,s gershonS Gershon,

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    A placebo-controlled, random-assignment, parallel-group pilot study of adjunctive topiramate for patients with schizoaffective disorder, bipolar type. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Bipolar disorders

    VOLUME: 9

    Page Numbers: 609-17

    Journal Abbreviation: Bipolar Disord

    ISSN: 1398-5647

    DAY: 11

    MONTH: Sep

    YEAR: 2007

    A placebo-controlled, random-assignment, parallel-group pilot study of adjunctive topiramate for patients with schizoaffective disorder, bipolar type. Information

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    LANGUAGE: eng

    NlmUniqueID: 100883596

    A placebo-controlled, random-assignment, parallel-group pilot study of adjunctive topiramate for patients with schizoaffective disorder, bipolar type. Keywords Mesh Terms:

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    Grant and Affiliation Information for A placebo-controlled, random-assignment, parallel-group pilot study of adjunctive topiramate for patients with schizoaffective disorder, bipolar type.

    AFFILIATION: Western Psychiatric Institute and Clinic, School of Medicine, University of Pittsburgh, and Mayview State Hospital, Pittsburgh, PA, USA. chengappakn@upmc.edu

    Country: Denmark

    Denmark Research PublicationDenmark Research Publication

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    MEDLINETA: Bipolar Disord

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