Description Details Author(s) Examples
Computes the required sample size using the optimal designs with multiple constraints proposed in Mayo et al.(2010). This optimal method is designed for two-arm, randomized phase II clinical trials, and the required sample size can be optimized either using fixed or flexible randomization allocation ratios.
Package: | SampleSize_OptimalDesign |
Type: | Package |
Version: | 1.0 |
Date: | 2013-12-03 |
License: | GPL-2 |
Wei Jiang, Jonathan Mahnken, Matthew Mayo Maintainer: Wei Jiang<wjiang@kumc.edu>
1 2 | Sample.Size(0.3, 0.6, 0.15, 0.15, 0.15, Allratio_c = 1, Allratio_e = 3)
Sample.Size(0.3, 0.6, 0.15, 0.15, 0.15)
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Specified values for parameters:
Response rates:
control = 0.3 experiment = 0.6
Upper bounds for constriants:
gammaC = 0.15 gammaE = 0.15 gammaDelta = 0.15
Required sample sizes:
[1] Optimal Design:
nc = 20 ne = 20 n = 40
[2] 1 to 1 Allocation Design:
nc = 20 ne = 20 n = 40
[3] 1 to 3 Allocation Design:
nc = 13 ne = 39 n = 52
Specified values for parameters:
Response rates:
control = 0.3 experiment = 0.6
Upper bounds for constriants:
gammaC = 0.15 gammaE = 0.15 gammaDelta = 0.15
Required sample sizes:
[1] Optimal Design:
nc = 20 ne = 20 n = 40
[2] 1 to 1 Allocation Design:
nc = 20 ne = 20 n = 40
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