Augmenting the logrank test in the design of clinical trials in which non-proportional hazards of the treatment effect may be anticipated

Title
Augmenting the logrank test in the design of clinical trials in which non-proportional hazards of the treatment effect may be anticipated
Authors
Keywords
Time-to-event data, Randomized controlled trials, Hazard ratio, Restricted mean survival time, Non-proportional hazards, Logrank test, Permutation test, Design, Simulation, Flexible parametric model
Journal
BMC Medical Research Methodology
Volume 16, Issue 1, Pages -
Publisher
Springer Nature
Online
2016-02-11
DOI
10.1186/s12874-016-0110-x

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