Literature DB >> 6671121

Optimal crossover designs in the presence of carryover effects.

E Laska, M Meisner, H B Kushner.   

Abstract

Under either the random patient-effect model with sequence effects or the fixed patient-effect model, the usual two-period, two-treatment crossover design, AB,BA, cannot be used to estimate the contrast between direct treatment effects when unequal carryover effects are present. If baseline observations are available, the design AB,BA can validly be used to estimate a treatment contrast. However, the design AB,BA,AA,BB with baseline observations is more efficient. In fact, we show that this design is optimal whether or not baseline observations are available. For experiments with more than two periods, universally optimal designs are found for both models, with and without carryover effects. It is shown that uncertainty about the presence of carryover effects is of little or no consequence, and the addition of baseline observations is of little or no added value for designs with three or more periods; however, if the experiment is limited to only two periods the investigator pays a heavy penalty.

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Year:  1983        PMID: 6671121

Source DB:  PubMed          Journal:  Biometrics        ISSN: 0006-341X            Impact factor:   2.571


  2 in total

1.  Cost-efficient higher-order crossover designs in comparative bioavailability studies.

Authors:  Jihao Zhou; Ying Yuan; Rebecca Reynolds; Susan Raber; Youjuan Li
Journal:  Clin Pharmacokinet       Date:  2006       Impact factor: 6.447

2.  Novel Modelling Approaches to Characterize and Quantify Carryover Effects on Sensory Acceptability.

Authors:  Damir Dennis Torrico; Wannita Jirangrat; Jing Wang; Penkwan Chompreeda; Sujinda Sriwattana; Witoon Prinyawiwatkul
Journal:  Foods       Date:  2018-11-08
  2 in total

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