• B G Charlton.
• Department of Epidemiology and Public Health, University of Newcastle upon Tyne.
• J R Coll Physicians Lond. 1995 Mar 1; 29 (2): 96-100.

AbstractA recent development of the therapeutic trial has been the mega-trial: a large, simple randomised trial analysed on an 'intention to treat' basis. Mega-trials have advantages in terms of increased statistical power, but also raise several new questions of interpretation. In mega-trials, randomisation serves to achieve identical allocation groups in a situation where there is poor experimental control and a large measure of between-subject variation. The results of mega-trials cannot readily be generalised because their conclusions are observations, not casual hypotheses, and are therefore not testable. In this sense, mega-trials can be repeated but cannot be replicated. Basic science and clinical science both seek understanding at the level of the individual subject; but in a mega-trial, analysis is only meaningful at the group level. The non-scientific nature of mega-trials derives from their methodology, which dispenses with the scientific aim of maximum experimental control to remove or minimise bias, and instead uses randomisation to achieve an equal distribution of bias between groups.

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