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      Meta-analyses involving cross-over trials: methodological issues.

      International Journal of Epidemiology
      Cross-Over Studies, Humans, Meta-Analysis as Topic, Randomized Controlled Trials as Topic, Review Literature as Topic

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          Abstract

          Meta-analysis of randomized controlled trials (RCTs) is usually based on trials where patients are randomized individually into two different, parallel, treatment groups. This paper concentrates on RCTs of a different design-two-period, two-treatment cross-over trials. The characteristics of these trials are outlined, with detailed examples of methods for analysis for both continuous and binary data. These case studies are then extended into the context of a meta-analysis. The Cochrane Library was surveyed to assess current practice for synthesis. Methods are described for continuous and binary data for use both when the necessary paired data are given and also when they need to be calculated or imputed, and some suggestions are provided to help people wishing to synthesize data from cross-over trials into meta-analyses. The survey suggested that about 8% of the trials in the Cochrane library were cross-over trials and 18% of the reviews referred to such trials, although there was no consistent approach to their inclusion into the reviews. Methods do exist for including valuable information from two-period, two-treatment cross-over trials into quantitative reviews. However, poor reporting of cross-over trials will often impede attempts to perform a meta-analysis using the available methods.

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          Most cited references17

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          The two-period cross-over clinical trial.

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            People and eyes: statistical approaches in ophthalmology.

            In conclusion, when an observation by its nature involves two eyes, as for blindness, statistical analyses should be conducted on individuals rather than eyes and between eye correlation is not a problem. In other circumstances, if information on only one eye per individual is used in the analysis there is a potential "waste" of information leading to less precise estimates of effect and less power. In addition, bias may be introduced into a study if there is non-random selection of the eye for inclusion in the analysis. The use of an overall summary of ocular findings for an individual may result in "wastage" of information in a similar fashion to the use of only one eye per individual. On the other hand, an analysis of individual eyes with no allowance made for between eye correlation may result in falsely narrow confidence intervals around estimates of effect. Between eyes correlation may be assessed empirically using the kappa statistic or similar means. If between eye correlation is substantial, statistical techniques exist which can utilise all available data while allowing for the correlation. In some circumstances a powerful design may be to use the fellow eye as a "control". Two conclusions may be drawn from this review of analytical approaches to the analysis of clinical data in the BJO. Firstly, the analytical approaches employed in many studies fail to use all the data available. In other words the analysis is less than "optimal". Secondly, in a proportion of studies, inappropriate statistical methods are used which may lead the investigator to draw inappropriate conclusions. In other words, the analysis is invalid. Ophthalmic data, by their very nature, present particular statistical challenges. We emphasise the need to involve appropriate statistical expertise in the design and analysis of ophthalmic studies.
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              THE TWO-PERIOD CHANGE-OVER DESIGN AN ITS USE IN CLINICAL TRIALS.

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                Author and article information

                Journal
                11914310
                10.1093/ije/31.1.140

                Chemistry
                Cross-Over Studies,Humans,Meta-Analysis as Topic,Randomized Controlled Trials as Topic,Review Literature as Topic

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