Literature DB >> 11653993

Ethics and statistics in randomized clinical trials.

Richard M Royall, Robert H Bartlett, Richard G Cornell, David P Byar, William D Dupont, Robert J Levine, Foster Lindley, R John Simes, M Zelen.   

Abstract

Keywords:  Biomedical and Behavioral Research; Empirical Approach

Mesh:

Year:  1991        PMID: 11653993     DOI: 10.1214/ss/1177011934

Source DB:  PubMed          Journal:  Stat Sci        ISSN: 0883-4237            Impact factor:   2.901


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  11 in total

Review 1.  Ethical problems of evaluating a new treatment for melioidosis.

Authors:  Allen C Cheng; Michael Lowe; Dianne P Stephens; Bart J Currie
Journal:  BMJ       Date:  2003-11-29

2.  The epistemology and ethics of chronic disease research: further lessons from ECMO.

Authors:  Robyn Bluhm
Journal:  Theor Med Bioeth       Date:  2010-04

Review 3.  Statistics and ethics: models for strengthening protection of human subjects in clinical research.

Authors:  Christine K Cassel
Journal:  Proc Natl Acad Sci U S A       Date:  2009-12-22       Impact factor: 11.205

Review 4.  Practical Bayesian adaptive randomisation in clinical trials.

Authors:  Peter F Thall; J Kyle Wathen
Journal:  Eur J Cancer       Date:  2007-02-16       Impact factor: 9.162

Review 5.  Adaptive designs for randomized trials in public health.

Authors:  C Hendricks Brown; Thomas R Ten Have; Booil Jo; Getachew Dagne; Peter A Wyman; Bengt Muthén; Robert D Gibbons
Journal:  Annu Rev Public Health       Date:  2009       Impact factor: 21.981

6.  Bandit solutions provide unified ethical models for randomized clinical trials and comparative effectiveness research.

Authors:  William H Press
Journal:  Proc Natl Acad Sci U S A       Date:  2009-12-14       Impact factor: 11.205

7.  Clinical and prophylactic trials with assured new treatment for those at greater risk: I. A design proposal.

Authors:  M O Finkelstein; B Levin; H Robbins
Journal:  Am J Public Health       Date:  1996-05       Impact factor: 9.308

8.  Challenges of clinical trial design when there is lack of clinical equipoise: use of a response-conditional crossover design.

Authors:  Chunqin Deng; Kim Hanna; Vera Bril; Marinos C Dalakas; Peter Donofrio; Pieter A van Doorn; Hans-Peter Hartung; Ingemar S J Merkies
Journal:  J Neurol       Date:  2011-08-07       Impact factor: 4.849

9.  Informed consent and research design in critical care medicine.

Authors: 
Journal:  Crit Care       Date:  1999       Impact factor: 9.097

Review 10.  Are adaptive randomised trials or non-randomised studies the best way to address the Ebola outbreak in west Africa?

Authors:  Simone Lanini; Alimuddin Zumla; John P A Ioannidis; Antonino Di Caro; Sanjeev Krishna; Lawrence Gostin; Enrico Girardi; Michel Pletschette; Gino Strada; Aldo Baritussio; Gina Portella; Giovanni Apolone; Silvio Cavuto; Roberto Satolli; Peter Kremsner; Francesco Vairo; Giuseppe Ippolito
Journal:  Lancet Infect Dis       Date:  2015-04-14       Impact factor: 25.071

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