Subgroup analyses in randomised controlled trials: cohort study on trial protocols and journal publications

نویسندگان

  • Benjamin Kasenda
  • Stefan Schandelmaier
  • Xin Sun
  • Erik von Elm
  • John You
  • Anette Blümle
  • Yuki Tomonaga
  • Ramon Saccilotto
  • Alain Amstutz
  • Theresa Bengough
  • Joerg J Meerpohl
  • Mihaela Stegert
  • Kelechi K Olu
  • Kari A O Tikkinen
  • Ignacio Neumann
  • Alonso Carrasco-Labra
  • Markus Faulhaber
  • Sohail M Mulla
  • Dominik Mertz
  • Elie A Akl
  • Dirk Bassler
  • Jason W Busse
  • Ignacio Ferreira-González
  • Francois Lamontagne
  • Alain Nordmann
  • Viktoria Gloy
  • Heike Raatz
  • Lorenzo Moja
  • Rachel Rosenthal
  • Shanil Ebrahim
  • Per O Vandvik
  • Bradley C Johnston
  • Martin A Walter
  • Bernard Burnand
  • Matthias Schwenkglenks
  • Lars G Hemkens
  • Heiner C Bucher
  • Gordon H Guyatt
  • Matthias Briel
چکیده

OBJECTIVE To investigate the planning of subgroup analyses in protocols of randomised controlled trials and the agreement with corresponding full journal publications. DESIGN Cohort of protocols of randomised controlled trial and subsequent full journal publications. SETTING Six research ethics committees in Switzerland, Germany, and Canada. DATA SOURCES 894 protocols of randomised controlled trial involving patients approved by participating research ethics committees between 2000 and 2003 and 515 subsequent full journal publications. RESULTS Of 894 protocols of randomised controlled trials, 252 (28.2%) included one or more planned subgroup analyses. Of those, 17 (6.7%) provided a clear hypothesis for at least one subgroup analysis, 10 (4.0%) anticipated the direction of a subgroup effect, and 87 (34.5%) planned a statistical test for interaction. Industry sponsored trials more often planned subgroup analyses compared with investigator sponsored trials (195/551 (35.4%) v 57/343 (16.6%), P<0.001). Of 515 identified journal publications, 246 (47.8%) reported at least one subgroup analysis. In 81 (32.9%) of the 246 publications reporting subgroup analyses, authors stated that subgroup analyses were prespecified, but this was not supported by 28 (34.6%) corresponding protocols. In 86 publications, authors claimed a subgroup effect, but only 36 (41.9%) corresponding protocols reported a planned subgroup analysis. CONCLUSIONS Subgroup analyses are insufficiently described in the protocols of randomised controlled trials submitted to research ethics committees, and investigators rarely specify the anticipated direction of subgroup effects. More than one third of statements in publications of randomised controlled trials about subgroup prespecification had no documentation in the corresponding protocols. Definitive judgments regarding credibility of claimed subgroup effects are not possible without access to protocols and analysis plans of randomised controlled trials.

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Subgroup analyses in randomised controlled trials: cohort study on trial protocols and journal publications

Objective To investigate the planning of subgroup analyses in protocols of randomised controlled trials and the agreement with corresponding full journal publications. DesignCohort of protocols of randomised controlled trial and subsequent full journal publications. Setting Six research ethics committees in Switzerland, Germany, and Canada. Data sources 894 protocols of randomised controlled tr...

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عنوان ژورنال:

دوره 349  شماره 

صفحات  -

تاریخ انتشار 2014