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Updated: Aug 18, 2026

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Inadequacy of sample sizes in clinical trials of laboratory parameters attributable to invalid statistical
1Center for Imaging and Pharmaceutical Research, Massachusetts General Hospital, Charlestown 02129.
Abstract:
Clinical trials often determine the sample size based on the use of statistical methods such as analysis of variance, t tests, and rank sum tests, which compare mean or median values. The resulting studies rarely are big enough to show that the method is based on mistaken assumptions. Data from a recent clinical trial of nephrotoxicity associated with the use of contrast agents during angiography found a significant difference on the order of the difference that previous studies had intended to detect. It also showed that a central assumption does not apply to changes in serum creatinine. As a result, the previous studies had considerably lower power than believed. Their lack of significance reflected only the mistaken assumption. Analysis of variance, t tests, and rank sum tests may be just as invalid for other clinical parameters. Lack of significance cannot be automatically taken to imply a small treatment effect.
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