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Trial protocols at the BMJ
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Trial protocols at the BMJ (2004)Trial protocols at the BMJIdentifying outcome reporting bias in randomised trials on PubMed: review of publications and survey of authors (2005)Identifying outcome reporting…Compulsory registration of clinical trials (2005)Compulsory registration of cl…Outcome reporting bias in randomized trials funded by the Canadian Institutes of Health Research (2004)Outcome reporting bias in ran…Empirical Evidence for Selective Reporting of Outcomes in Randomized Trials (2004)Empirical Evidence for Select…Improving the quality of reports of meta-analyses of randomised controlled trials: the QUOROM statement (1999)Improving the quality of repo…Improving the quality of reporting of randomized controlled trials. The CONSORT statement (1998)Improving the quality of repo…Improving the quality of reporting of randomized controlled trials. The CONSORT statement (1996)Improving the quality of repo…A scoping review identifies multiple comments suggesting modifications to SPIRIT 2013 and CONSORT 2010 (2023)A scoping review identifies m…SPIRIT 2013 Bildirisi: Klinik Deneyler İçin Standart Protokol Maddelerinin Tanımlanması (2021)SPIRIT 2013 Bildirisi: Klinik…The natural history of conducting and reporting clinical trials: interviews with trialists (2015)The natural history of conduc…Systematic Reviews: Identifying relevant studies for systematic reviews (1994)Empirical evidence of bias. Dimensions of methodological quality associated with estimates of treatment effects in controlled trials (1995)Assessing the quality of reports of randomized clinical trials: Is blinding necessary? (1996)A Systematic Evaluation of the Impact of STRICTA and CONSORT Recommendations on Quality of Reporting for Acupuncture Trials (2008)Research Review: Recommendations for reporting on treatment trials for child and adolescent anxiety disorders – an international consensus statement (2020)CONSORT 2025 statement: Updated guideline for reporting randomised trials (2025)Empirical Evidence of Bias (1995)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 (2009)Preferred reporting items for systematic reviews and meta-analyses: the PRISMA Statement. (2009)Registering Clinical Trials (2003)CONSORT 2010 Explanation and Elaboration: updated guidelines for reporting parallel group randomised trials (2010)SPIRIT 2013 explanation and elaboration: guidance for protocols of clinical trials (2013)SPIRIT 2013 Statement: Defining Standard Protocol Items for Clinical Trials (2013)COMPare: Qualitative analysis of researchers’ responses to critical correspondence on a cohort of 58 misreported trials (2019)Barriers and Facilitating Factors for Conducting Systematic Evidence Assessments in Academic Clinical Trials (2021)Registry versus publication: discrepancy of primary outcomes and possible outcome reporting bias in child and adolescent mental health (2021)The CONSORT statement: revised recommendations for improving the quality of reports of parallel group randomized trials (2001)The CONSORT statement: revised recommendations for improving the quality of reports of parallel-group randomised trials (2001)The Revised CONSORT Statement for Reporting Randomized Trials: Explanation and Elaboration (2001)Trial sequential analysis may establish when firm evidence is reached in cumulative meta-analysis (2007)Contour-enhanced meta-analysis funnel plots help distinguish publication bias from other causes of asymmetry (2008)CONSORT 2010 Statement: updated guidelines for reporting parallel group randomised trials (2010)Meta-analyses involving cross-over trials: methodological issues (2002)Bias in Clinical Intervention Research (2006)Cognitive behavioural therapy for anxiety disorders in children and adolescents (2015)Acceptance and Commitment Therapy (ACT) for Chronic Pain (2016)Statistical Methods for Examining Heterogeneity and Combining Results from Several Studies in Meta‐Analysis (2001)Meta‐Analysis Of Controlled Clinical Trials (2002)A systematic review identifies a lack of standardization in methods for handling missing variance data (2006)STrengthening the REporting of Genetic Association studies (STREGA) – an extension of the STROBE statement (2009)STrengthening the REporting of Genetic Association Studies (STREGA)—an extension of the STROBE statement (2009)CONSORT 2010 Statement: Updated Guidelines for Reporting Parallel Group Randomized Trials (2010)CONSORT 2010 Statement: updated guidelines for reporting parallel group randomised trials (2010)PRISMA Extension for Scoping Reviews (PRISMA-ScR): Checklist and Explanation (2018)Development of a topic‐specific bibliographic database supporting the updates of SPIRIT 2013 and CONSORT 2010 (2024)Does quality of reports of randomised trials affect estimates of intervention efficacy reported in meta-analyses? (1998)Core outcome domains for chronic pain clinical trials: IMMPACT recommendations (2003)Strengthening the Reporting of Observational Studies in Epidemiology (STROBE): Explanation and Elaboration (2007)
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References

  • 1999Improving the quality of reports of meta-analyses of randomised controlled trials: the QUOROM statement4,828 cited
  • 1996Improving the quality of reporting of randomized controlled trials. The CONSORT statement3,337 cited
  • 2004Empirical Evidence for Selective Reporting of Outcomes in Randomized Trials1,845 cited
  • 2005Identifying outcome reporting bias in randomised trials on PubMed: review of publications and survey of authors612 cited
  • 2004Outcome reporting bias in randomized trials funded by the Canadian Institutes of Health Research442 cited
  • 1998Improving the quality of reporting of randomized controlled trials. The CONSORT statement177 cited
  • 2005Compulsory registration of clinical trials36 cited

Cited by

  • 2015The natural history of conducting and reporting clinical trials: interviews with trialists32 cited
  • 2023A scoping review identifies multiple comments suggesting modifications to SPIRIT 2013 and CONSORT 201020 cited
  • 2021SPIRIT 2013 Bildirisi: Klinik Deneyler İçin Standart Protokol Maddelerinin Tanımlanması17 cited

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