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Reporting transparency and completeness in trials: Paper 4 - reporting of randomised controlled trials conducted using routinely collected electronic records – room for improvement
16 references·1 citing·35 second hop
Reporting transparency and completeness in trials: Paper 4 - reporting of randomised controlled trials conducted using routinely collected electronic records – room for improvement (2021)Reporting transparency and completeness i…CONSORT extension for the reporting of randomised controlled trials conducted using cohorts and routinely collected data (CONSORT-ROUTINE): checklist with explanation and elaboration (2021)CONSORT extension for the rep…Reporting of Multi-Arm Parallel-Group Randomized Trials (2019)Reporting of Multi-Arm Parall…The reporting of studies using routinely collected health data was often insufficient (2016)The reporting of studies usin…PRESS Peer Review of Electronic Search Strategies: 2015 Guideline Statement (2016)PRESS Peer Review of Electron…CONSORT 2010 statement: extension to randomised pilot and feasibility trials (2016)CONSORT 2010 statement: exten…The REporting of studies Conducted using Observational Routinely-collected health Data (RECORD) Statement (2015)The REporting of studies Cond…Evidence summaries: the evolution of a rapid review approach (2012)Evidence summaries: the evolu…Does use of the CONSORT Statement impact the completeness of reporting of randomised controlled trials published in medical journals? A Cochrane reviewa (2012)Does use of the CONSORT State…Consolidated standards of reporting trials (CONSORT) and the completeness of reporting of randomised controlled trials (RCTs) published in medical journals (2012)Consolidated standards of rep…CONSORT 2010 Statement: updated guidelines for reporting parallel group randomised trials (2010)CONSORT 2010 Statement: updat…CONSORT 2010 Statement: updated guidelines for reporting parallel group randomised trials (2010)CONSORT 2010 Statement: updat…CONSORT 2010 Explanation and Elaboration: updated guidelines for reporting parallel group randomised trials (2010)CONSORT 2010 Explanation and …CONSORT 2010 Explanation and Elaboration: updated guidelines for reporting parallel group randomised trials (2010)CONSORT 2010 Explanation and …Does quality of reports of randomised trials affect estimates of intervention efficacy reported in meta-analyses? (1998)Does quality of reports of ra…Empirical evidence of bias. Dimensions of methodological quality associated with estimates of treatment effects in controlled trials (1995)Empirical evidence of bias. D…Empirical Evidence of Bias (1995)Empirical Evidence of BiasPaper II: thematic framework analysis of registry-based randomized controlled trials provided insights for designing trial ready registries (2023)Paper II: thematic framework …The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) Statement: Guidelines for Reporting Observational Studies (2007)The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) Statement: Guidelines for Reporting Observational Studies (2007)CONSORT 2010 Statement: Updated Guidelines for Reporting Parallel Group Randomized Trials (2010)SPIRIT 2013 explanation and elaboration: guidance for protocols of clinical trials (2013)Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement (2009)Preferred reporting items for systematic reviews and meta-analyses: the PRISMA Statement. 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(2012)Response rates for CBT for anxiety disorders: Need for standardized criteria (2015)Dealing with missing standard deviation and mean values in meta-analysis of continuous outcomes: a systematic review (2018)
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References

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  • 2010CONSORT 2010 Explanation and Elaboration: updated guidelines for reporting parallel group randomised trials8,873 cited
  • 2015The REporting of studies Conducted using Observational Routinely-collected health Data (RECORD) Statement5,686 cited
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628 cited
  • 2019Reporting of Multi-Arm Parallel-Group Randomized Trials321 cited
  • 2021CONSORT extension for the reporting of randomised controlled trials conducted using cohorts and routinely collected data (CONSORT-ROUTINE): checklist with explanation and elaboration139 cited
  • 2016The reporting of studies using routinely collected health data was often insufficient73 cited
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    • 2023Paper II: thematic framework analysis of registry-based randomized controlled trials provided insights for designing trial ready registries7 cited