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# Author: dlabes
# -----------------------------------------------------------------------------
library(PowerTOST)
# function to create sample size tables
sampsiz <- function(alpha=0.05, power, CV, GMR, theta1, logscale=TRUE,
design="2x2", method="exact")
{
# 'cartesian' product
data <- merge(CV, GMR)
names(data) <- c("CV","GMR")
tbl <- data.frame()
for (j in seq_along(power))
{
data$n <- 1
data$power <- power[j]
for (i in seq_along(data$n)) {
data$n[i] <- sampleN.TOST(alpha=alpha, CV=data[i,"CV"],
theta0=data$GMR[i], logscale=logscale,
targetpower=power[j], theta1=theta1,
design=design, method=method,
print=FALSE)[,"Sample size"]
}
data2 <- reshape(data, v.names="n", idvar=c("power","CV"), timevar="GMR",
direction="wide")
names(data2) <- gsub("n.","R",names(data2))
names(data2)[names(data2)=="R1"] <- "R1.0"
names(data2)[names(data2)=="R0"] <- "R0.0"
cat("Power",power[j],"\n")
print(data2[,-2],row.names=FALSE)
cat("\n")
tbl <- rbind(tbl, data2)
}
return(invisible(tbl))
}
# Chow and Liu use a model with carry-over, i.e. a degree of freedom
# which is one less than in PowerTOST
cat(paste('Chow S.C., Liu J.P.\n',
'"Design and Analysis of Bioavailability\n',
'and Bioequvalence Studies", Third edition\n',
'CRC Press, Chapman & Hall, Boca Raton (2009)\n\n',sep=""))
cat("Table 9.6.4 2x4x4, BEL 0.8-1.20, additive model,\n")
cat("approximate via shifted central t-distribution\n")
CVs <- seq(from=0.1, to=0.4, by=0.02)
GMRs <- seq(from=0.0, to=0.15, by=0.05)
power <- c(0.8, 0.9)
t9.6.4 <- sampsiz(power=power, CV=CVs, GMR=GMRs, logscale=FALSE, theta1=-0.2,
method="shifted", design="2x4x4")
cat("Table 9.6.8 2x4x4, BEL 0.8-1.25, multiplicative model model,\n");
cat("approximate via shifted central t-distribution\n")
cat("Attention! Liu, Chow's CV is se!\n")
se <- seq(from=0.1, to=0.4, by=0.02)
CVs <- se2CV(se)
GMRs <- seq(from=0.85, to=1.2, by=0.05)
power <- c(0.8, 0.9)
t9.6.8 <- sampsiz(power=power, CV=CVs, GMR=GMRs, logscale=TRUE, theta1=0.8,
method="shift", design="2x4x4")
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