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Assay sensitivity is a property of a clinical trial defined as the ability of a trial to distinguish an effective treatment from a less effective or ineffective intervention.[1] Without assay sensitivity, a trial is not internally valid and is not capable of comparing the efficacy of two interventions.
- ^ Chuang-Stein, Christy (2014), "Assay Sensitivity", Wiley StatsRef: Statistics Reference Online, American Cancer Society, doi:10.1002/9781118445112.stat07119, ISBN 978-1-118-44511-2, retrieved 2020-01-21