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Journal Abstract Search
162 related items for PubMed ID: 12520557
41. A comparison of multiple testing procedures for the gold standard non-inferiority trial. Röhmel J, Pigeot I. J Biopharm Stat; 2010 Sep; 20(5):911-26. PubMed ID: 20721781 [Abstract] [Full Text] [Related]
42. Bayesian approach to the design and analysis of non-inferiority trials for anti-infective products. Gamalo MA, Tiwari RC, LaVange LM. Pharm Stat; 2014 Sep; 13(1):25-40. PubMed ID: 23913880 [Abstract] [Full Text] [Related]
43. Operating characteristics of sample size re-estimation with futility stopping based on conditional power. Lachin JM. Stat Med; 2006 Oct 15; 25(19):3348-65. PubMed ID: 16345019 [Abstract] [Full Text] [Related]
44. Sample size re-estimation in group-sequential response-adaptive clinical trials. Morgan CC. Stat Med; 2003 Dec 30; 22(24):3843-57. PubMed ID: 14673942 [Abstract] [Full Text] [Related]
45. Therapeutic equivalence: fallacies and falsification. Garrett AD. Stat Med; 2003 Mar 15; 22(5):741-62. PubMed ID: 12587103 [Abstract] [Full Text] [Related]
46. Choice of lambda-margin and dependency of non-inferiority trials. Tsong Y, Levenson M, Zhang J, Zhong J. Stat Med; 2008 Feb 20; 27(4):520-8. PubMed ID: 17617797 [Abstract] [Full Text] [Related]
47. Re-formulating non-inferiority trials as superiority trials: The case of binary outcomes. Durkalski VL, Berger VW. Biom J; 2009 Feb 20; 51(1):185-92. PubMed ID: 19197960 [Abstract] [Full Text] [Related]
48. Sample size estimation for non-inferiority trials of time-to-event data. Crisp A, Curtis P. Pharm Stat; 2008 Feb 20; 7(4):236-44. PubMed ID: 17583558 [Abstract] [Full Text] [Related]
49. Flexible two-stage design with sample size reassessment for survival trials. Desseaux K, Porcher R. Stat Med; 2007 Nov 30; 26(27):5002-13. PubMed ID: 17577242 [Abstract] [Full Text] [Related]
50. Pairwise non-parametric non-inferiority tests in 3 x 3 cross-over trials: should we adjust for period? Duchateau L, Janssen P. Stat Med; 2005 May 30; 24(10):1525-36. PubMed ID: 15761908 [Abstract] [Full Text] [Related]
51. A comparison of intent-to-treat and per-protocol results in antibiotic non-inferiority trials. Brittain E, Lin D. Stat Med; 2005 Jan 15; 24(1):1-10. PubMed ID: 15532089 [Abstract] [Full Text] [Related]
52. Assessment of blinding in clinical trials. Bang H, Ni L, Davis CE. Control Clin Trials; 2004 Apr 15; 25(2):143-56. PubMed ID: 15020033 [Abstract] [Full Text] [Related]
53. Exact unconditional tests for testing non-inferiority in matched-pairs design. Sidik K. Stat Med; 2003 Jan 30; 22(2):265-78. PubMed ID: 12520561 [Abstract] [Full Text] [Related]
54. Evaluation of the statistical power for multiple tests: a case study. Yeo A, Qu Y. Pharm Stat; 2009 Jan 30; 8(1):5-11. PubMed ID: 18381588 [Abstract] [Full Text] [Related]
55. Increasing the sample size when the unblinded interim result is promising. Chen YH, DeMets DL, Lan KK. Stat Med; 2004 Apr 15; 23(7):1023-38. PubMed ID: 15057876 [Abstract] [Full Text] [Related]
56. Methodology of superiority vs. equivalence trials and non-inferiority trials. Christensen E. J Hepatol; 2007 May 15; 46(5):947-54. PubMed ID: 17412447 [Abstract] [Full Text] [Related]
57. Determining equivalence and the impact of sample size in anti-infective studies: a point to consider. Bristol DR. J Biopharm Stat; 1996 Jul 15; 6(3):319-26. PubMed ID: 8854235 [Abstract] [Full Text] [Related]
58. Group sequential t-test for clinical trials with small sample sizes across stages. Shao J, Feng H. Contemp Clin Trials; 2007 Sep 15; 28(5):563-71. PubMed ID: 17434814 [Abstract] [Full Text] [Related]
59. Statistical considerations of FDA and CPMP rules for the investigation of new anti-bacterial products. Röhmel J. Stat Med; 2007 Sep 15; 20(17-18):2561-71. PubMed ID: 11523069 [Abstract] [Full Text] [Related]
60. ['Non-inferiority' trials. Tips for the critical reader. Research methodology 3]. Soonawala D, Dekkers OM. Ned Tijdschr Geneeskd; 2012 Sep 15; 156(19):A4665. PubMed ID: 22571548 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]