174 related articles for article (PubMed ID: 27936355)
1. Sample size determination for a three-arm equivalence trial of Poisson and negative binomial responses.
Chang YW; Tsong Y; Zhao Z
J Biopharm Stat; 2017; 27(2):239-256. PubMed ID: 27936355
[TBL] [Abstract][Full Text] [Related]
2. Sample size determination for a three-arm equivalence trial of normally distributed responses.
Chang YW; Tsong Y; Dong X; Zhao Z
J Biopharm Stat; 2014; 24(6):1190-202. PubMed ID: 25098678
[TBL] [Abstract][Full Text] [Related]
3. Sample size for comparing negative binomial rates in noninferiority and equivalence trials with unequal follow-up times.
Tang Y
J Biopharm Stat; 2018; 28(3):475-491. PubMed ID: 28541744
[TBL] [Abstract][Full Text] [Related]
4. Sample size calculation for comparing two negative binomial rates.
Zhu H; Lakkis H
Stat Med; 2014 Feb; 33(3):376-87. PubMed ID: 24038204
[TBL] [Abstract][Full Text] [Related]
5. Sample size determination for equivalence assessment with multiple endpoints.
Sun A; Dong X; Tsong Y
J Biopharm Stat; 2014; 24(6):1203-14. PubMed ID: 25032845
[TBL] [Abstract][Full Text] [Related]
6. On sample size requirement for analytical similarity assessment.
Zhao Y; Chang YW; Chow SC
J Biopharm Stat; 2018; 28(6):1143-1159. PubMed ID: 29513612
[TBL] [Abstract][Full Text] [Related]
7. Sample size determination for assessing equivalence based on proportion ratio under a randomized trial with non-compliance and missing outcomes.
Lui KJ; Chang KC
Stat Med; 2008 Jan; 27(1):47-67. PubMed ID: 17708514
[TBL] [Abstract][Full Text] [Related]
8. Modeling motor vehicle crashes using Poisson-gamma models: examining the effects of low sample mean values and small sample size on the estimation of the fixed dispersion parameter.
Lord D
Accid Anal Prev; 2006 Jul; 38(4):751-66. PubMed ID: 16545328
[TBL] [Abstract][Full Text] [Related]
9. Study design for a three-arm equivalence clinical trial with binomially distributed outcomes.
Tseng YK; Hsu KN
J Biopharm Stat; 2021 Nov; 31(6):736-744. PubMed ID: 34460350
[TBL] [Abstract][Full Text] [Related]
10. Blinded sample size recalculation in clinical trials incorporating historical data.
Hees K; Kieser M
Contemp Clin Trials; 2017 Dec; 63():2-7. PubMed ID: 28735110
[TBL] [Abstract][Full Text] [Related]
11. Regional consistency and sample size considerations in a multiregional equivalence trial.
Wu SC; Xu JF; Zhang XJ; Li ZW; He J
Pharm Stat; 2020 Nov; 19(6):897-908. PubMed ID: 32716135
[TBL] [Abstract][Full Text] [Related]
12. Design and analysis of three-arm trials with negative binomially distributed endpoints.
Mütze T; Munk A; Friede T
Stat Med; 2016 Feb; 35(4):505-21. PubMed ID: 26388314
[TBL] [Abstract][Full Text] [Related]
13. Sizing clinical trials when comparing bivariate time-to-event outcomes.
Sugimoto T; Hamasaki T; Evans SR; Sozu T
Stat Med; 2017 Apr; 36(9):1363-1382. PubMed ID: 28120524
[TBL] [Abstract][Full Text] [Related]
14. A noniterative sample size procedure for tests based on t distributions.
Tang Y
Stat Med; 2018 Sep; 37(22):3197-3213. PubMed ID: 29876954
[TBL] [Abstract][Full Text] [Related]
15. A U-statistics based approach to sample size planning of two-arm trials with discrete outcome criterion aiming to establish either superiority or noninferiority.
Wellek S
Stat Med; 2017 Feb; 36(5):799-812. PubMed ID: 27878839
[TBL] [Abstract][Full Text] [Related]
16. A studentized permutation test for three-arm trials in the 'gold standard' design.
Mütze T; Konietschke F; Munk A; Friede T
Stat Med; 2017 Mar; 36(6):883-898. PubMed ID: 27859506
[TBL] [Abstract][Full Text] [Related]
17. Group sequential design and analysis of clinical equivalence assessment for generic nonsystematic drug products.
Tsong Y; Zhang JJ; Wang SJ
J Biopharm Stat; 2004 May; 14(2):359-73. PubMed ID: 15206533
[TBL] [Abstract][Full Text] [Related]
18. Selection of the effect size for sample size determination for a continuous response in a superiority clinical trial using a hybrid classical and Bayesian procedure.
Ciarleglio MM; Arendt CD; Peduzzi PN
Clin Trials; 2016 Jun; 13(3):275-85. PubMed ID: 26928986
[TBL] [Abstract][Full Text] [Related]
19. Study duration for three-arm non-inferiority survival trials designed for accrual by cohorts.
Wu Y; Li Y; Hou Y; Li K; Zhou X
Stat Methods Med Res; 2018 Feb; 27(2):507-520. PubMed ID: 26994213
[TBL] [Abstract][Full Text] [Related]
20. Equivalence and superiority testing in regeneration clinical trials.
Gunsolley JC; Elswick RK; Davenport JM
J Periodontol; 1998 May; 69(5):521-7. PubMed ID: 9623894
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
