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A Clinical Trial Assessing the Safety, Efficacy, and Delivery of Olive-Oil-Based Three-Chamber Bags for Parenteral Nutrition
Published on: September 20, 2019
Non-inferiority trial design for recurrent events
Richard J Cook1, Ker-Ai Lee, Hongdan Li
1Department of Statistics and Actuarial Science, University of Waterloo, 200 University Avenue West, Waterloo, ON, Canada N2L 3G1.
Abstract:
We describe methods for designing non-inferiority trials with recurrent event responses arising from mixed-Poisson models. Sample size formulae are derived for trials in which treatment effects are expressed as relative rates and as absolute differences in cumulative mean functions at a particular time. Simulation studies are conducted to provide empirical validation of the frequency properties of the design and testing procedures under the null and alternative hypotheses using both mixed-Poisson models and robust marginal methods. The robustness of the design to mis-specification of the random effect distribution is also studied empirically. Sample size requirements based on the proposed method are contrasted with those from a design based on the time to the first event for a motivating study of patients with bone metastases at risk of skeletal complications. When the between-patient heterogeneity in the event rate is small, there may be a considerable reduction in sample size with recurrent event outcomes.
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