Literature DB >> 8493420

Behind closed doors: the data monitoring board in randomized clinical trials.

J Wittes1.   

Abstract

Many randomized clinical trials include a data and safety monitoring board (DSMB) that is responsible for reviewing accruing data, monitoring performance of the trial, assuring safety of the participants in the trial, and assessing the efficacy of treatment. The DSMB often makes recommendations about continuation of the trial or alteration of the protocol. Although such boards are very influential in both the conduct and interpretation of randomized clinical trials, there is no standard mode in which DSMBs operate nor do they routinely report publicly about their deliberations. This paper describes the composition of DSMBs as well as their functions. It concludes with a series of questions that needs to be addressed to ensure that the DSMBs operate effectively.

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Year:  1993        PMID: 8493420     DOI: 10.1002/sim.4780120504

Source DB:  PubMed          Journal:  Stat Med        ISSN: 0277-6715            Impact factor:   2.373


  4 in total

1.  Funding evidence: the National Institute of Neurological Disorders and Stroke Clinical Trials Program.

Authors:  Bernard Ravina; Scott Janis; Julianna Keleti; John M Marler
Journal:  NeuroRx       Date:  2004-07

Review 2.  Reporting of data monitoring boards in publications of randomized clinical trials is often deficient: ACTTION systematic review.

Authors:  Jennifer S Gewandter; Rachel A Kitt; Matthew R Hunsinger; Joseph Poku; Jacqueline Lozano; Jenna Chaudari; Scott Evans; Robert A Gross; Michael P McDermott; Michael C Rowbotham; Dennis C Turk; Robert H Dworkin
Journal:  J Clin Epidemiol       Date:  2017-01-23       Impact factor: 6.437

3.  External data required timely response by the Trial Steering-Data Monitoring Committee for the NALoxone InVEstigation (N-ALIVE) pilot trial.

Authors:  Sheila M Bird; John Strang; Deborah Ashby; John Podmore; J Roy Robertson; Sarah Welch; Angela M Meade; Mahesh K B Parmar
Journal:  Contemp Clin Trials Commun       Date:  2017-03

4.  Quantitative Framework for Retrospective Assessment of Interim Decisions in Clinical Trials.

Authors:  Roger Stanev
Journal:  Med Decis Making       Date:  2016-06-27       Impact factor: 2.583

  4 in total

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