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. Author manuscript; available in PMC: 2019 Nov 27.
Published in final edited form as: J Biopharm Stat. 2015;25(4):812–829. doi: 10.1080/10543406.2014.920858

Table 3.

Power (percent) for detecting a treatment effect based on 4000 simulations in a two-arm (placebo/treatment) parallel design study, by μ and the standard deviation of the values after treatment (σTrt) Results are for at least 99% of the simulations, except as indicated.

μ (64 per arm, σTrt = 1) μ (90 per arm, σTrt = 1.4)
2.0 2.5 3.0 4.0 2.0 2.5 3.0 4.0
Model
Nonparametric analyses
Wilcoxon test (NQ only) 60.3 74.0 75.8 76.8 38.9 60.5 70.1 77.0
Wilcoxon test (both NQ and ND) 67.9 79.0 76.9 76.8 53.2 68.2 72.7 77.1
Gehan test (NQ only) 61.0 74.9 76.8 78.0 36.7 60.3 71.5 77.1
Mixed models using both baseline and follow-up data
Equal variances 82.3 90.5 92.1 93.2 37.7 63.2 81.6 93.8
Unequal variances 77.0 89.9 92.4 93.1 64.2 81.4 90.8 94.5
Mixture models using likelihood L2 and follow-up data only
Equal variances 51.6 63.5 67.1 56.1d NS NS NS NS
Unequal variances 51.4 61.5 63.6 51.7d NS NS NS NS
Mixture models using likelihood L2 and both baseline and follow-up data
Equal variances 19.8c 25.1b 26.6a 30.6a NS NS NS NS
Unequal variances 28.2c 33.2b 30.7a 25.1a NS NS NS NS
Generalized estimating equation logistic regression models for a significant decrease
NQ and ND combined 36.2 52.7 67.1 68.3 17.7 41.0 65.2 83.3
ND separate from NQ 52.5 64.5 71.4 68.8 33.5 55.2 72.0 84.0

Assumptions: treatment reduces the underlying mean μ by 0.5, the standard deviation of the untreated mean is 1, and Type I error is 0.05. Quantification limit is log10(80) = 1.90. NQ: non-quantifiable; ND: not detectable.

NQ only: NQ and ND were combined.

a

Results for 90% to 98.9% of all simulations.

b

Results for 80% to 89.9% of all simulations.

c

Results for 70% to 79.9% of all simulations.

d

Results for 60% to 69.9% of all simulations.

NS: not shown, excessive Type I error.