CONSORT 2010 Statement: updated guidelines for reporting parallel group randomized trials
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[1] Tom Starzl,et al. THE LANCET , 1992, The Lancet.
[2] Curtis L. Meinert,et al. A proposal for structured reporting of randomized controlled trials. The Standards of Reporting Trials Group. , 1994, JAMA.
[3] D. Rennie. Reporting randomized controlled trials. An experiment and a call for responses from readers. , 1995, JAMA.
[4] R. J. Hayes,et al. Empirical evidence of bias. Dimensions of methodological quality associated with estimates of treatment effects in controlled trials. , 1995, JAMA.
[5] I. Olkin,et al. Improving the quality of reporting of randomized controlled trials. The CONSORT statement. , 1996, JAMA.
[6] N. Black. CONSORT , 1996, The Lancet.
[7] D. Cook,et al. Does quality of reports of randomised trials affect estimates of intervention efficacy reported in meta-analyses? , 1998, The Lancet.
[8] S. Casswell,et al. What is meant by intention to treat analysis? Survey of published randomised controlled trials , 1999 .
[9] G. Morrison,et al. University of Pennsylvania School of Medicine. , 2000, Academic medicine : journal of the Association of American Medical Colleges.
[10] David Moher,et al. The CONSORT statement: revised recommendations for improving the quality of reports of parallel group randomized trials , 2001, Annals of Internal Medicine.
[11] D. Moher,et al. The CONSORT statement: revised recommendations for improving the quality of reports of parallel-group randomized trials. , 2001, Journal of the American Podiatric Medical Association.
[12] Douglas G Altman,et al. Systematic reviews in health care: Assessing the quality of controlled clinical trials. , 2001, BMJ.
[13] Kenneth F Schulz,et al. Blinding in randomised trials: hiding who got what , 2002, The Lancet.
[14] Joy Melnikow,et al. Reporting number needed to treat and absolute risk reduction in randomized controlled trials. , 2002, JAMA.
[15] David Moher,et al. Towards complete and accurate reporting of studies of diagnostic accuracy: the STARD initiative. Standards for Reporting of Diagnostic Accuracy. , 2003, Clinical chemistry.
[16] Douglas G. Altman,et al. The CONSORT statement: revised recommendations for improving the quality of reports of parallel-group randomised trials , 2001, The Lancet.
[17] B. Djulbegovic,et al. Pharmaceutical industry sponsorship and research outcome and quality: systematic review , 2003, BMJ : British Medical Journal.
[18] A. Walker,et al. Improving the quality of reporting in randomised controlled trials. , 2004, Journal of wound care.
[19] A. Hrõbjartsson,et al. Empirical evidence for selective reporting of outcomes in randomized trials: comparison of protocols to published articles. , 2004, JAMA.
[20] J. Ioannidis,et al. Better Reporting of Harms in Randomized Trials: An Extension of the CONSORT Statement , 2004, Annals of Internal Medicine.
[21] R. Horton,et al. Clinical trial registration: a statement from the International Committee of Medical Journal Editors. , 2005, Circulation research.
[22] D. Altman,et al. CONSORT statement: extension to cluster randomised trials , 2004, BMJ : British Medical Journal.
[23] Clinical trial registration: a statement from the International Committee of Medical Journal Editors , 2004, The Lancet.
[24] John Hoey,et al. Clinical trial registration: a statement from the International Committee of Medical Journal Editors. , 2004, JAMA.
[25] David Moher,et al. Towards complete and accurate reporting of studies of diagnostic accuracy: the STARD initiative. , 2004, Family practice.
[26] Gordon H Guyatt,et al. Randomized trials stopped early for benefit: a systematic review. , 2005, JAMA.
[27] John Hoey,et al. Clinical trial registration: a statement from the International Committee of Medical Journal Editors. , 2004, JAMA.
[28] Douglas G Altman,et al. Epidemiology and reporting of randomised trials published in PubMed journals , 2005, The Lancet.
[29] Peter C Gøtzsche,et al. [Better reporting of harms in randomized trials: an extension of the CONSORT statement]. , 2005, Ugeskrift for laeger.
[30] D. Moher,et al. Does the CONSORT checklist improve the quality of reports of randomised controlled trials? A systematic review , 2006, The Medical journal of Australia.
[31] Douglas G Altman,et al. Reporting of noninferiority and equivalence randomized trials: an extension of the CONSORT statement. , 2006, JAMA.
[32] David Moher,et al. Reporting Randomized, Controlled Trials of Herbal Interventions: An Elaborated CONSORT Statement , 2006, Annals of Internal Medicine.
[33] David L Sackett,et al. Commentary: Measuring the success of blinding in RCTs: don't, must, can't or needn't? , 2007, International journal of epidemiology.
[34] Douglas G Altman,et al. Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies. , 2008, BMJ.
[35] S. Pocock,et al. The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement: guidelines for reporting observational studies. , 2007, Preventive medicine.
[36] Matthias Egger,et al. The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) Statement: Guidelines for Reporting Observational Studies , 2007, PLoS medicine.
[37] Douglas G Altman,et al. The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) Statement: guidelines for reporting observational studies. , 2014, International journal of surgery.
[38] D. Moher,et al. Extending the CONSORT statement to randomized trials of nonpharmacologic treatment: explanation and elaboration. , 2008, Annals of internal medicine.
[39] Carl Heneghan,et al. What is missing from descriptions of treatment in trials and reviews? , 2008, BMJ : British Medical Journal.
[40] T. Wachs,et al. CONSORT for reporting randomised trials in journal and conference abstracts , 2008 .
[41] David Moher,et al. [CONSORT for reporting randomized controlled trials in journal and conference abstracts: explanation and elaboration]. , 2008, Zhong xi yi jie he xue bao = Journal of Chinese integrative medicine.
[42] D. Moher,et al. CONSORT for reporting randomised trials in journal and conference abstracts , 2008, The Lancet.
[43] J. Ioannidis,et al. Systematic Review of the Empirical Evidence of Study Publication Bias and Outcome Reporting Bias , 2008, PloS one.
[44] D. Moher,et al. Improving the reporting of pragmatic trials: an extension of the CONSORT statement , 2008, BMJ : British Medical Journal.
[45] D. Moher,et al. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement , 2009, BMJ.
[46] D. Moher,et al. CONSORT 2010 Explanation and Elaboration: updated guidelines for reporting parallel group randomised trials , 2010, BMJ : British Medical Journal.
[47] David Moher,et al. CONSORT 2010 changes and testing blindness in RCTs , 2010, The Lancet.
[48] Jeremy Howick,et al. What's in Placebos: Who Knows? Analysis of Randomized, Controlled Trials , 2010, Annals of Internal Medicine.
[49] D. Moher,et al. CONSORT 2010 explanation and elaboration: updated guidelines for reporting parallel group randomised trials. , 2012, International journal of surgery.
[50] Sally Hopewell,et al. The quality of reports of randomised trials in 2000 and 2006: comparative study of articles indexed in PubMed , 2010, BMJ : British Medical Journal.
[51] D. Moher,et al. CONSORT 2010 Statement: updated guidelines for reporting parallel group randomised trials , 2010, BMC medicine.
[52] S. Pocock,et al. Reporting of noninferiority and equivalence randomized trials: extension of the CONSORT 2010 statement. , 2006, JAMA.