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    Results: 1 to 20 of 337

    1.

    A comparison of missing data methods for hypothesis tests of the treatment effect in substance abuse clinical trials: a Monte-Carlo simulation study.

    Hedden SL, Woolson RF, Malcolm RJ.

    Subst Abuse Treat Prev Policy. 2008 Jun 3;3:13.

    PMID:
    18522752
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    2.

    The impact of loss to follow-up on hypothesis tests of the treatment effect for several statistical methods in substance abuse clinical trials.

    Hedden SL, Woolson RF, Carter RE, Palesch Y, Upadhyaya HP, Malcolm RJ.

    J Subst Abuse Treat. 2009 Jul;37(1):54-63. Epub 2008 Nov 13.

    PMID:
    19008067
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    3.

    A simulation study of estimators for rates of change in longitudinal studies with attrition.

    Wang-Clow F, Lange M, Laird NM, Ware JH.

    Stat Med. 1995 Feb 15;14(3):283-97.

    PMID:
    7724914
    [PubMed - indexed for MEDLINE]
    4.

    Assessing missing data assumptions in longitudinal studies: an example using a smoking cessation trial.

    Yang X, Shoptaw S.

    Drug Alcohol Depend. 2005 Mar 7;77(3):213-25.

    PMID:
    15734221
    [PubMed - indexed for MEDLINE]
    5.
    6.

    Randomization in substance abuse clinical trials.

    Hedden SL, Woolson RF, Malcolm RJ.

    Subst Abuse Treat Prev Policy. 2006 Feb 6;1:6. Review.

    PMID:
    16722591
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    7.

    Clinical trial optimization: Monte Carlo simulation Markov model for planning clinical trials recruitment.

    Abbas I, Rovira J, Casanovas J.

    Contemp Clin Trials. 2007 May;28(3):220-31. Epub 2006 Aug 10.

    PMID:
    16979387
    [PubMed - indexed for MEDLINE]
    8.

    Testing for robustness in Monte Carlo studies.

    Serlin RC.

    Psychol Methods. 2000 Jun;5(2):230-40.

    PMID:
    10937332
    [PubMed - indexed for MEDLINE]
    9.

    Identifying the types of missingness in quality of life data from clinical trials.

    Curran D, Bacchi M, Schmitz SF, Molenberghs G, Sylvester RJ.

    Stat Med. 1998 Mar 15-Apr 15;17(5-7):739-56. Review.

    PMID:
    9549820
    [PubMed - indexed for MEDLINE]
    10.

    Test for interaction between treatment and stratum with ordinal responses.

    Uesaka H.

    Biometrics. 1993 Mar;49(1):123-9.

    PMID:
    8513097
    [PubMed - indexed for MEDLINE]
    11.

    Power of automated algorithms for combining time-line follow-back and urine drug screening test results in stimulant-abuse clinical trials.

    Oden NL, VanVeldhuisen PC, Wakim PG, Trivedi MH, Somoza E, Lewis D.

    Am J Drug Alcohol Abuse. 2011 Sep;37(5):350-7.

    PMID:
    21854277
    [PubMed - indexed for MEDLINE]
    12.

    Exemplary data: sample size and power in the design of event-time clinical trials.

    Goldman AI, Hillman DW.

    Control Clin Trials. 1992 Aug;13(4):256-71.

    PMID:
    1330432
    [PubMed - indexed for MEDLINE]
    13.

    Power analyses for longitudinal study designs with missing data.

    Tu XM, Zhang J, Kowalski J, Shults J, Feng C, Sun W, Tang W.

    Stat Med. 2007 Jul 10;26(15):2958-81.

    PMID:
    17154250
    [PubMed - indexed for MEDLINE]
    14.

    Imputation methods for missing outcome data in meta-analysis of clinical trials.

    Higgins JP, White IR, Wood AM.

    Clin Trials. 2008;5(3):225-39.

    PMID:
    18559412
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    15.

    An overview of practical approaches for handling missing data in clinical trials.

    DeSouza CM, Legedza AT, Sankoh AJ.

    J Biopharm Stat. 2009 Nov;19(6):1055-73. Review.

    PMID:
    20183464
    [PubMed - indexed for MEDLINE]
    16.

    Intention-to-treat: methods for dealing with missing values in clinical trials of progressively deteriorating diseases.

    Unnebrink K, Windeler J.

    Stat Med. 2001 Dec 30;20(24):3931-46.

    PMID:
    11782044
    [PubMed - indexed for MEDLINE]
    17.

    Design and analysis of group sequential logrank tests in maximum duration versus information trials.

    Kim K, Boucher H, Tsiatis AA.

    Biometrics. 1995 Sep;51(3):988-1000.

    PMID:
    7548714
    [PubMed - indexed for MEDLINE]
    18.

    Weibull prediction of event times in clinical trials.

    Ying GS, Heitjan DF.

    Pharm Stat. 2008 Apr-Jun;7(2):107-20.

    PMID:
    17377932
    [PubMed - indexed for MEDLINE]
    19.

    Practical usage of O'Brien's OLS and GLS statistics in clinical trials.

    Dallow NS, Leonov SL, Roger JH.

    Pharm Stat. 2008 Jan-Mar;7(1):53-68.

    PMID:
    17390306
    [PubMed - indexed for MEDLINE]
    20.

    Sequential analysis of latent variables using mixed-effect latent variable models: Impact of non-informative and informative missing data.

    Sébille V, Hardouin JB, Mesbah M.

    Stat Med. 2007 Nov 30;26(27):4889-904.

    PMID:
    17576119
    [PubMed - indexed for MEDLINE]

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