GenTwoArmsTrialSize
CRANGenTwoArmsTrialSizeMaRDI QIDQ5979059FDOQ5979059
Generalized Two Arms Clinical Trial Sample Size Calculation
Mohsen Soltanifar, Chel Hee Lee
Last update: 11 December 2023
Copyright license: GNU General Public License, version 3.0
Software version identifier: 0.0.4.3, 0.0.4.4, 0.0.4.5
Two arms clinical trials required sample size is calculated in the comprehensive parametric context. The calculation is based on the type of endpoints(continuous/binary/time-to-event/ordinal), design (parallel/crossover), hypothesis tests (equality/noninferiority/superiority/equivalence), trial arms noncompliance rates and expected loss of follow-up. Methods are described in: Chow SC, Shao J, Wang H, Lokhnygina Y (2017) <doi:10.1201/9781315183084>, Wittes, J (2002) <doi:10.1093/epirev/24.1.39>, Sato, T (2000) <doi:10.1002/1097-0258(20001015)19:19%3C2689::aid-sim555%3E3.0.co;2-0>, Lachin J M, Foulkes, M A (1986) <doi:10.2307/2531201>, Whitehead J(1993) <doi:10.1002/sim.4780122404>, Julious SA (2023) <doi:10.1201/9780429503658>.
- Evaluation of Sample Size and Power for Analyses of Survival with Allowance for Nonuniform Patient Entry, Losses to Follow-Up, Noncompliance, and Stratification
- Sample Size Calculations in Clinical Research: Third Edition
- Sample Size Calculations for Randomized Controlled Trials
- Sample size calculations with compliance information
- Sample size calculations for ordered categorical data
- Sample Sizes for Clinical Trials
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