These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
169 related articles for article (PubMed ID: 9789917)
1. Using prior information to allocate significance levels for multiple endpoints. Westfall PH; Krishen A; Young SS Stat Med; 1998 Sep; 17(18):2107-19. PubMed ID: 9789917 [TBL] [Abstract][Full Text] [Related]
2. Sample size determination with familywise control of both type I and type II errors in clinical trials. Wang B; Ting N J Biopharm Stat; 2016; 26(5):951-65. PubMed ID: 26881972 [TBL] [Abstract][Full Text] [Related]
3. Power and sample size for clinical trials when efficacy is required in multiple endpoints: application to an Alzheimer's treatment trial. Xiong C; Yu K; Gao F; Yan Y; Zhang Z Clin Trials; 2005; 2(5):387-93. PubMed ID: 16317808 [TBL] [Abstract][Full Text] [Related]
4. Bayesian sample size calculations for a non-inferiority test of two proportions in clinical trials. Daimon T Contemp Clin Trials; 2008 Jul; 29(4):507-16. PubMed ID: 18201944 [TBL] [Abstract][Full Text] [Related]
5. Sample size re-estimation incorporating prior information on a nuisance parameter. Mütze T; Schmidli H; Friede T Pharm Stat; 2018 Mar; 17(2):126-143. PubMed ID: 29181869 [TBL] [Abstract][Full Text] [Related]
6. A Bayesian predictive sample size selection design for single-arm exploratory clinical trials. Teramukai S; Daimon T; Zohar S Stat Med; 2012 Dec; 31(30):4243-54. PubMed ID: 22807115 [TBL] [Abstract][Full Text] [Related]
7. Bayesian multiple testing for two-sample multivariate endpoints. Gönen M; Westfall PH; Johnson W Biometrics; 2003 Mar; 59(1):76-82. PubMed ID: 12762443 [TBL] [Abstract][Full Text] [Related]
8. Sample size estimation in single-arm clinical trials with multiple testing under frequentist and Bayesian approaches. Zaslavsky BG; Scott J J Biopharm Stat; 2012; 22(4):819-35. PubMed ID: 22651117 [TBL] [Abstract][Full Text] [Related]
10. Bayesian sample size calculations in phase II clinical trials using informative conjugate priors. Mayo MS; Gajewski BJ Control Clin Trials; 2004 Apr; 25(2):157-67. PubMed ID: 15020034 [TBL] [Abstract][Full Text] [Related]
11. Sample size and the probability of a successful trial. Chuang-Stein C Pharm Stat; 2006; 5(4):305-9. PubMed ID: 17128428 [TBL] [Abstract][Full Text] [Related]
12. A Method for Constructing Informative Priors for Bayesian Modeling of Occupational Hygiene Data. Quick H; Huynh T; Ramachandran G Ann Work Expo Health; 2017 Jan; 61(1):67-75. PubMed ID: 28395307 [TBL] [Abstract][Full Text] [Related]
13. Multiplicity-adjusted sample size requirements: a strategy to maintain statistical power with Bonferroni adjustments. Leon AC J Clin Psychiatry; 2004 Nov; 65(11):1511-4. PubMed ID: 15554764 [TBL] [Abstract][Full Text] [Related]
15. Ignorance is not bliss: Statistical power is not probability of trial success. Zierhut ML; Bycott P; Gibbs MA; Smith BP; Vicini P Clin Pharmacol Ther; 2016 Apr; 99(4):356-9. PubMed ID: 26331445 [TBL] [Abstract][Full Text] [Related]
16. Bayesian design and analysis of composite endpoints in clinical trials with multiple dependent binary outcomes. Zaslavsky BG Pharm Stat; 2013; 12(4):207-12. PubMed ID: 23625660 [TBL] [Abstract][Full Text] [Related]
18. Robust meta-analytic-predictive priors in clinical trials with historical control information. Schmidli H; Gsteiger S; Roychoudhury S; O'Hagan A; Spiegelhalter D; Neuenschwander B Biometrics; 2014 Dec; 70(4):1023-32. PubMed ID: 25355546 [TBL] [Abstract][Full Text] [Related]
19. Power and sample size when multiple endpoints are considered. Senn S; Bretz F Pharm Stat; 2007; 6(3):161-70. PubMed ID: 17674404 [TBL] [Abstract][Full Text] [Related]
20. Evaluation of the statistical power for multiple tests: a case study. Yeo A; Qu Y Pharm Stat; 2009; 8(1):5-11. PubMed ID: 18381588 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]