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Clinical trials should employ an ITT analysis strategy, comprising a design that attempts to follow up all randomised individuals, a main analysis that is valid under a stated plausible assumption about the missing data, and sensitivity analyses that include all randomised individuals in order to explore the impact of departures from the assumption underlying the main analysis. Following this strategy recognises the extra uncertainty arising from missing outcomes and increases the incentive for researchers to minimise the extent of missing data.
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White et al. (Mon,) studied this question.
synapsesocial.com/papers/69dcd1ca2e182f147e133432 — DOI: https://doi.org/10.1177/1740774512450098
Ian R. White
John Innes Centre
James R. Carpenter
London School of Hygiene & Tropical Medicine
Nicholas J. Horton
Amherst College
Clinical Trials
London School of Hygiene & Tropical Medicine
University of London
MRC Biostatistics Unit
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