RSS-Feed abonnieren
Bitte kopieren Sie die angezeigte URL und fügen sie dann in Ihren RSS-Reader ein.
https://www.thieme-connect.de/rss/thieme/de/10.1055-s-00000011.xml
Dtsch Med Wochenschr 2011; 136(8): e20-e23
DOI: 10.1055/s-0031-1272980
DOI: 10.1055/s-0031-1272980
Kommentar | Commentary
Medizinisches Publizieren
© Georg Thieme Verlag KG Stuttgart · New York
CONSORT 2010: Aktualisierte Leitlinie für Berichte randomisierter Studien im Parallelgruppen-Design
CONSORT 2010 statement: updated guidelines for reporting parallel group randomised trialsWeitere Informationen
Publikationsverlauf
Publikationsdatum:
10. Februar 2011 (online)
Die Autoren der bearbeiteten Übersetzung aus dem Englischen sind: M. H. Pittler1, A. Blümle1, J. J. Meerpohl1,2, G. Antes1
1Deutsches Cochrane Zentrum, Abteilung
für Medizinische Biometrie und Statistik,
Universitätsklinikum Freiburg, Freiburg
2Pädiatrische Hämatologie und Onkologie,
Zentrum für Kinder- und Jugendmedizin,
Universitätsklinikum Freiburg, Freiburg
Literatur
- 1 Begg C, Cho M, Eastwood S. et al . Improving the quality of reporting of randomized controlled trials. The CONSORT statement. JAMA. 1996; 276 637-639
- 2 Boutron I, Moher D, Altman D G, Schulz K F, Ravaud P. Extending the CONSORT statement to randomized trials of nonpharmacologic treatment: explanation and elaboration. Ann Intern Med. 2008; 148 295-309
- 3 Campbell M K, Elbourne D R, Altman D G. CONSORT statement: extension to cluster randomised trials. BMJ. 2004; 328 702-708
- 4 Chan A W, Hrobjartsson A, Haahr M T, Gotzsche P C, Altman D G. Empirical evidence for selective reporting of outcomes in randomized trials: comparison of protocols to published articles. JAMA. 2004; 291 2457-2465
- 5 De Angelis C, Drazen J M, Frizelle F A. et al . Clinical trial registration: a statement from the International Committee of Medical Journal Editors. Ann Intern Med. 2004; 141 477-478
- 6 Dwan K, Altman D G, Arnaiz J A. et al . Systematic review of the empirical evidence of study publication bias and outcome reporting bias. PLoS ONE. 2008; 3 e3081
- 7 Gagnier J J, Boon H, Rochon P. et al . Reporting randomized, controlled trials of herbal interventions: an elaborated CONSORT statement. Ann Intern Med. 2006; 144 364-367
- 8 Glasziou P, Meats E, Heneghan C, Shepperd S. What is missing from descriptions of treatment in trials and reviews?. BMJ. 2008; 336 1472-1474
- 9 Hollis S, Campbell F. What is meant by intention to treat analysis? Survey of published randomised controlled trials. BMJ. 1999; 319 670-674
- 10 Hopewell S, Clarke M, Moher D. et al . CONSORT for reporting randomised trials in journal and conference abstracts. Lancet. 2008; 371 281-283
- 11 Hopewell S, Clarke M, Moher D. et al . CONSORT for reporting randomized controlled trials in journal and conference abstracts: explanation and elaboration. PLoS Med. 2008; 5 e20
- 12 Ioannidis J P, Evans S J, Gotzsche P C. et al . Better reporting of harms in randomized trials: an extension of the CONSORT statement. Ann Intern Med. 2004; 141 781-788
- 13 Lexchin J, Bero L A, Djulbegovic B, Clark O. Pharmaceutical industry sponsorship and research outcome and quality: systematic review. BMJ. 2003; 326 1167-1170
- 14 Moher D, Hopewell S, Schulz K F. et al . CONSORT 2010 explanation and elaboration: updated guidelines for reporting parallel group randomised trials. BMJ. 2010; 340 c869
- 15 Moher D, Schulz K F, Altman D G, Gruppe f dC. Das CONSORT Statement: Überarbeitete Empfehlungen zur Qualitätsverbesserung von Reports randomisierter Studien im Parallel-Design. Dtsch med Wochenschr. 2004; 129 T16-T20
- 16 Montori V M, Devereaux P J, Adhikari N K. et al . Randomized trials stopped early for benefit: a systematic review. JAMA. 2005; 294 2203-2209
- 17 Nuovo J, Melnikow J, Chang D. Reporting number needed to treat and absolute risk reduction in randomized controlled trials. JAMA. 2002; 287 2813-2814
- 18 Piaggio G, Elbourne D R, Altman D G, Pocock S J, Evans S J. Reporting of noninferiority and equivalence randomized trials: an extension of the CONSORT statement. JAMA. 2006; 295 1152-1160
- 19 Sackett D L. Commentary: Measuring the success of blinding in RCTs: don’t, must, can’t or needn’t?. Int J Epidemiol. 2007; 36 664-665
- 20 Schulz K F, Altman D G, Moher D. for the CONSORT Group . CONSORT 2010 Statement: updated guidelines for reporting parallel group randomised trials. BMJ. 2010; 340 c332
- 21 Schulz K F, Grimes D A. Blinding in randomised trials: hiding who got what. The Lancet. 2002; 359 696-700
- 22 Zwarenstein M, Treweek S, Gagnier J J. et al . Improving the reporting of pragmatic trials: an extension of the CONSORT statement. BMJ. 2008; 337 a2390
Dr. Gerd Antes
Deutsches Cochrane Zentrum
Abteilung für
Medizinische Biometrie und Statistik
Institut
für Medizinische Biometrie und Medizinische Informatik
Universitätsklinikum
Freiburg
Berliner Allee 29
79110 Freiburg
eMail: antes@cochrane.de