Journal
BIOMARKERS
Volume 8, Issue 1, Pages 13-32Publisher
TAYLOR & FRANCIS LTD
DOI: 10.1080/1354750021000039389
Keywords
surrogate endpoints; design; power; NNT
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The randomized controlled trial (RCT) is scientific experiment during which observations on the effects of therapy or preventive action are conducted by the researcher under rigorous control. The purpose of the experiment is to clear the uncertainties surrounding clinical/research issue and involves isolating the treatment and end result variables from external influences. RCTs therefore make use of scientific method standards: measuring, which includes the possibility of reproducing observations; controlling factors unconnected to the cause-effect relationship of interest; and the external veri cation or falsi cation of the cause-effect relationship. Many RCTs are now including biomarkers to answer scientific questions in more accurate way. In the present methodological paper, the main aspects involved in the design and conduction of trial are discussed, with special emphasis on the use of biomarkers. Aspects that are often overlooked by scientists involved in the design of trials include multiple comparisons, subgroup analysis, the duration of the observations, the use of surrogate endpoints, and ethical issues. This review summarizes the main issues that should be addressed in protocol, and illustrates these with an example.
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