Information and information fractions for design and sequential monitoring of clinical trials
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Publication:4843737
DOI10.1080/03610929408831263zbMath0825.62095OpenAlexW2070581312MaRDI QIDQ4843737
K. K. Gordon Lan, David L. Demets, David M. Reboussin
Publication date: 17 August 1995
Published in: Communications in Statistics - Theory and Methods (Search for Journal in Brave)
Full work available at URL: https://doi.org/10.1080/03610929408831263
Related Items (5)
An Efficient Allocation in Group Sequential Tests for the Linear Mixed Effects Model ⋮ An overview of group sequential methods in longitudinal clinical trials ⋮ Testing Secondary Hypotheses Following Sequential Clinical Trials ⋮ Basic concepts of group sequential and adaptive group sequential test procedures ⋮ Point estimation after early stopping in a repeated measures trial
Cites Work
- Random-Effects Models for Longitudinal Data
- Sequential analysis of the proportional hazards model
- Discrete Sequential Boundaries for Clinical Trials
- Evaluation of Sample Size and Power for Analyses of Survival with Allowance for Nonuniform Patient Entry, Losses to Follow-Up, Noncompliance, and Stratification
- The asymptotic joint distribution of the efficient scores test for the proportional hazards model calculated over time
- Sequential Clinical Trials for Normal Variates Using Interval Composite Hypotheses
- Sequential Monitoring for Comparison of Changes in a Response Variable in Clinical Studies
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