Design and analysis of cross-over trials
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(26)- Nonparametric testing under crossover design for ordered categorical response
- Robust assessment of two-treatment higher-order cross-over designs against missing values
- Design and Analysis of Crossover Trials for Absorbing Binary Endpoints
- scientific article; zbMATH DE number 45784 (Why is no real title available?)
- scientific article; zbMATH DE number 1907196 (Why is no real title available?)
- Multi-response based personalized treatment selection with data from crossover designs for multiple treatments
- Notes on power comparison between the sequential parallel comparison and other commonly-used designs
- Design and Analysis of Clinical Trials
- Design and Analysis of Bioavailability and Bioequivalence Studies
- Cross-over trials in drug development: Theory and practice
- Analysis of cross‐over experiments with count data in the presence of carry‐over effects
- A correlation structure for the analysis of Gaussian and non-Gaussian responses in crossover experimental designs with repeated measures
- Comparing treatment effects for the \textit{AB} : \textit{BA} crossover design with continuous responses: an alternative nonparametric approach
- Improving the efficiency of individually randomized clinical trials by staggering the introduction of the intervention
- Personalized treatment selection using data from crossover designs with carry-over effects
- Using population crossover trials to improve the decision process regarding treatment individualization in N-of-1 trials
- A Component-Position Model, Analysis and Design for Order-of-Addition Experiments
- Nonparametric tests for equality of two treatments for continuous responses under the standard two-period crossover design
- An objective Bayesian analysis of a crossover design via model selection and model averaging
- Simultaneous confidence regions for multivariate bioequivalence
- Two-stage test of means of unordered pairs
- Stepped wedge designs: insights from a design of experiments perspective
- Controlling the type I error rate in two-stage sequential adaptive designs when testing for average bioequivalence
- Penalized GEE for complex carry-over in repeated-measures crossover designs
- Adaptive two-treatment three-period crossover design for normal responses
- Approximate and exact designs for total effects
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