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Journal Abstract Search

715 related items for PubMed ID: 18264992

  • 1. Test equality and sample size calculation based on risk difference in a randomized clinical trial with noncompliance and missing outcomes.
    Lui KJ, Chang KC.
    Biom J; 2008 Apr; 50(2):224-36. PubMed ID: 18264992
    [Abstract] [Full Text] [Related]

  • 2. 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 15; 27(1):47-67. PubMed ID: 17708514
    [Abstract] [Full Text] [Related]

  • 3. Sample size determination for testing equality in a cluster randomized trial with noncompliance.
    Lui KJ, Chang KC.
    J Biopharm Stat; 2011 Jan 15; 21(1):1-17. PubMed ID: 21191850
    [Abstract] [Full Text] [Related]

  • 4. Estimation of the risk difference under a noncompliance randomized clinical trial with missing outcomes.
    Lui KJ.
    J Biopharm Stat; 2008 Jan 15; 18(2):273-92. PubMed ID: 18327721
    [Abstract] [Full Text] [Related]

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  • 6. Five interval estimators for proportion ratio under a stratified randomized clinical trial with noncompliance.
    Lui KJ, Chang KC.
    Biom J; 2007 Aug 15; 49(4):613-26. PubMed ID: 17634977
    [Abstract] [Full Text] [Related]

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  • 8. Sample size calculation in survival trials accounting for time-varying relationship between noncompliance and risk of outcome event.
    Li B, Grambsch P.
    Clin Trials; 2006 Aug 15; 3(4):349-59. PubMed ID: 17060209
    [Abstract] [Full Text] [Related]

  • 9. Interval estimation of the risk difference in non-compliance randomized trials with repeated binary measurements.
    Lui KJ.
    Stat Med; 2007 Jul 20; 26(16):3140-56. PubMed ID: 17177272
    [Abstract] [Full Text] [Related]

  • 10. Sample size determination for testing equality in Poisson frequency data under an AB/BA crossover trial.
    Lui KJ.
    Pharm Stat; 2013 Jul 20; 12(2):74-81. PubMed ID: 23364859
    [Abstract] [Full Text] [Related]

  • 11. Test homogeneity of odds ratio in a randomized clinical trial with noncompliance.
    Lui KJ, Chang KC.
    J Biopharm Stat; 2009 Sep 20; 19(5):916-32. PubMed ID: 20183452
    [Abstract] [Full Text] [Related]

  • 12. Interval estimation of risk ratio in the simple compliance randomized trial.
    Lui KJ.
    Contemp Clin Trials; 2007 Feb 20; 28(2):120-9. PubMed ID: 16820329
    [Abstract] [Full Text] [Related]

  • 13. Procedures for testing the homogeneity of relative difference in sparse data.
    Lui KJ.
    Stat Med; 2006 Feb 28; 25(4):685-97. PubMed ID: 16007573
    [Abstract] [Full Text] [Related]

  • 14. Likelihood methods for treatment noncompliance and subsequent nonresponse in randomized trials.
    O'Malley AJ, Normand SL.
    Biometrics; 2005 Jun 28; 61(2):325-34. PubMed ID: 16011678
    [Abstract] [Full Text] [Related]

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  • 16. Sample size estimation for GEE method for comparing slopes in repeated measurements data.
    Jung SH, Ahn C.
    Stat Med; 2003 Apr 30; 22(8):1305-15. PubMed ID: 12687656
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  • 18. Large sample tests for binary outcomes in fixed-dose combination drug studies.
    Wang SJ, Hung HM.
    Biometrics; 1997 Jun 30; 53(2):498-503. PubMed ID: 9192448
    [Abstract] [Full Text] [Related]

  • 19. Sample size determination for constrained longitudinal data analysis.
    Lu K, Mehrotra DV, Liu G.
    Stat Med; 2009 Feb 15; 28(4):679-99. PubMed ID: 19051207
    [Abstract] [Full Text] [Related]

  • 20. A general approach for sample size and statistical power calculations assessing of interventions using a mixture model in the presence of detection limits.
    Nie L, Chu H, Cole SR.
    Contemp Clin Trials; 2006 Oct 15; 27(5):483-91. PubMed ID: 16769254
    [Abstract] [Full Text] [Related]

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