Blinded and unblinded sample size reestimation in crossover trials balanced for period

Author:

Grayling Michael J.1ORCID,Mander Adrian P.1,Wason James M. S.1

Affiliation:

1. MRC Biostatistics Unit; Cambridge Institute of Public Health; Forvie Site, Robinson Way Cambridge UK

Funder

Medical Research Council

Publisher

Wiley

Subject

Statistics, Probability and Uncertainty,General Medicine,Statistics and Probability

Reference33 articles.

1. Optimal cross-over designs for full interaction models;Bailey;The Annals of Statistics,2014

2. European Medicines Agency (EMEA)-Committee for Medicinal Products for Human Use (CHMP) 2007 CHMP reflection paper on methodological issues in confirmatory clinical trials planned with an adaptive design

3. A multiple comparison procedure for comparing several treatments with a control;Dunnett;Journal of the American Statistical Association,1955

4. Food and Drug Administration (FDA) 2010 Guidance for industry-Adaptive design clinical trials for drugs and biologics

5. Applied Longitudinal Analysis

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