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    The publisher's final edited version of this article is available at Lancet flashes cite the published article.

    Others will see no improvement whatsoever. Titrate gabapentin higher as indicated for uncontrolled pain.

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    Max dose 1200 mg every 8 hours. Differences and percentage changes from baseline to week 4 or week 8 were calculated for each of the three measures.

    A mixed-effect model was used for comparison of the treatment effect on these measures.

    The fixed effects in the model included treatment group three strata, time two strata, 4 weeks and 8 weeks and baseline measures.

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    A random effect for participants was also included in the model. The assumptions made for mixed-effect models normality of error terms, mean, and covariance structure were checked thoroughly by use of residual plots.

    Outliers were identified and their influence on model estimation was examined.

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  • For purposes of comparison, simpler analyses were also done on change scores and percentage change scores at week 4 and week 8 separately, by ANCOVA. The drug and placebo were provided by Pfizer, Inc.

    The statistical package SAS for Windows, version 8 was younger for our analysis.
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    The study was reviewed and approved by the National Cancer Institute, but not by Pfizer, and neither funding source had any role in study design; collection, analysis, or interpretation of data; or the writing of the report.

    During the 4-week titration phase, patients were started on one 300-mg capsule of gabapentin or matching placebo.

    The causa of analysis was decided prospectively and deadly the intention-to-treat principle; data are coming in the treatment group to which a participant was assigned, irrespective of any but changes to the treatment.
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    METHODS: The study hypothesis was defined a priori as a lower 4-week migraine rate during the second stabilization period for the gabapentin-treated patients as compared with the placebo-treated patients.

    The analyses were performed with the 4-week migraine rate at baseline as a covariate and center as a blocking factor.

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