BMJ 1994;309:1007-1010 (15 October)
Education and debate
Systematic Reviews: Obtaining data from randomised controlled trials: how much do we need for reliable and informative meta-analyses?
M J Clarke,
L A Stewart
Clinical Trial Service Unit and ICRF Cancer Studies Unit, Radcliffe Infirmary, Oxford OX2 6HE MRC Cancer Trials Office, Cambridge CB2 2BW Correspondence to: Dr Clarke.
Many randomised controlled trials compare treatments that will produce only moderate differences in outcome, but these differences can be clinically important. However, they are difficult to assess reliably and require a large amount of randomised evidence. This can be achieved through large prospective randomised trials which will accrue future patients, the meta-analysis of results from randomised trials involving patients from the past, or - ideally - both. The techniques require that all possible biases are minimised, and in meta-analyses this can best be achieved by ensuring that all of the randomised evidence - both trials and participants in those trials - is included. The meta-analysis of individual patient data has been described as the gold standard for this approach. It will remove many of the problems associated with relying solely on published data and some of the problems arising from a reliance on aggregate data, and will also . . . [Full text of this article]

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