Last data update: 2014.03.03

R: Objects for handling with bi- and trifactorial trial data
carpetcubeR Documentation

Objects for handling with bi- and trifactorial trial data

Description

Create objects representing bi- or trifactorial clinical trial designs.

Usage

carpet(data,D,...)
cube(data,D,...)

Arguments

data

A list of numeric or binary data vectors from the trial. See the details below for the order in which the list is to be given.

D

An integer vector of length 2 for carpet objects and of length 3 for cube objects, specifying the number of doses of the components drugs in the trial.

...

Any further arguments.

Details

The function carpet creates objects of class carpet from the specified data in the list that are used row-wise to fill up the 2-factorial treatment groups, i.e. in the order (0,0), (0,1),..., (0,D[2]), (1,0), ..., (1,D[2]), ..., (D[1],D[2]); resulting in a (D[1]+1)x(D[2]+1) data array.

To represent trifactorial designs for the evaluation of a three-compound combination, an object of class cube can be created using the function cube. The data in the treatment groups are then filled up in the order (0,0,0), ..., (0,0,D[3]) first, then (0,1,0), ..., (0,1,D[3]) and up to (0,D[2],0), ..., (0,D[2],D[3]). This is the order also for the values 0, ..., D[1] for the first component group, always taking the data succesively from the list elements of data. The result is a (D[1]+1)x(D[2]+1)x(D[3]+1) data array. Methods for multiple inference and global tests can be applied to carpet and cube objects.

Value

An object of class carpet or cube, respectively, with the following slots.

data

The data list specified in the construction.

D

Vector of maximum doses specified in the construction.

n

Numeric vector of sample sizes in the respective groups.

Author(s)

Peter Frommolt, University of Cologne peter.frommolt@uni-koeln.de
http://portal.ccg.uni-koeln.de

References

Frommolt P, Hellmich M (2009): Resampling in multiple-dose factorial designs. Biometrical J, 51(6), pp. 915-31

Hung HMJ, Chi GYH, Lipicky RJ (1993): Testing for the existence of a desirable dose combination. Biometrics 49, pp. 85-94

Hung HMJ (2000): Evaluation of a combination drug with multiple doses in unbalanced factorial design clinical trials. Statistics in Medicine 19, pp. 2079-2087

See Also

bifactorial, mintest, margint, avetest, maxtest

Examples

#Hypertension example from Hung (2000)
data(sidbp)
x<-split(sidbp$ynrmhom,sidbp$cb)
bifactorial<-carpet(data=x,D=c(2,3))

Results