Cited by 289Pharmaceutical industry and healthcareAcademic integrity and plagiarismAcademic Publishing and Open Access

Ghost Authorship in Industry-Initiated Randomised Trials

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Gøtzsche, Peter C, Hróbjartsson, Asbjørn, Johansen, Helle Krogh, Haahr, Mette T, Altman, Douglas G, Chan, An-Wen·2007·PLoS Medicine

Abstract

BACKGROUND: Ghost authorship, the failure to name, as an author, an individual who has made substantial contributions to an article, may result in lack of accountability. The prevalence and nature of ghost authorship in industry-initiated randomised trials is not known. METHODS AND FINDINGS: We conducted a cohort study comparing protocols and corresponding publications for industry-initiated trials approved by the Scientific-Ethical Committees for Copenhagen and Frederiksberg in 1994-1995. We defined ghost authorship as present if individuals who wrote the trial protocol, performed the statistical analyses, or wrote the manuscript, were not listed as authors of the publication, or as members of a study group or writing committee, or in an acknowledgment. We identified 44 industry-initiated trials. We did not find any trial protocol or publication that stated explicitly that the clinical study report or the manuscript was to be written or was written by the clinical investigators, and none of the protocols stated that clinical investigators were to be involved with data analysis. We found evidence of ghost authorship for 33 trials (75%; 95% confidence interval 60%-87%). The prevalence of ghost authorship was increased to 91% (40 of 44 articles; 95% confidence interval 78%-98%) when we included cases where a person qualifying for authorship was acknowledged rather than appearing as an author. In 31 trials, the ghost authors we identified were statisticians. It is likely that we have overlooked some ghost authors, as we had very limited information to identify the possible omission of other individuals who would have qualified as authors. CONCLUSIONS: Ghost authorship in industry-initiated trials is very common. Its prevalence could be considerably reduced, and transparency improved, if existing guidelines were followed, and if protocols were publicly available.

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Research works printed but not linked: 2

  1. International Committee of Medical Journal Editors 2004 October Uniform requirements for manuscripts submitted to biomedical journals Philadelphia International Committee of Medical Journal Editors Available: http://www.icmje.org. Accessed 15 August 2006.
  2. Wager E Field EA Grossman L 2003 Good publication practice for pharmaceutical companies Curr Med Res Opin 19 149 154 12814125

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Authors
Gøtzsche, P. C., Hróbjartsson, A., Johansen, H. K., Haahr, M. T., Altman, D. G., & Chan, A.-W.
Affiliations
  • Cochrane (DK)
  • University of Oxford (GB)
  • University of Toronto (CA)
Corresponding author
Gøtzsche, Peter C
Venue
PLoS Medicine
Published
2007-01-16
Volume
4
Issue
1
Pages
e19
ISSN
  • 1549-1277 (ISSN-L)
  • 1549-1676
OpenAlex
W2095312096
Cited by
289
References
20
Citations by year
2026: 7 · 2025: 15 · 2024: 5 · 2023: 11 · 2022: 8 · 2021: 9 · 2020: 12 · 2019: 19 · 2018: 20 · 2017: 7 · 2016: 19 · 2015: 14 · 2014: 14 · 2013: 19 · 2012: 9
FWCI
25.09
Type
journal article
Language
en
Open access
Locations
  • PLoS Medicine (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • RePEc: Research Papers in Economics (acceptedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
  • DigitalGeorgetown (Georgetown University Library) (submittedVersion)
Funders
Cancer Research UK
Topics
  • Life Sciences › Pharmacology, Toxicology and Pharmaceutics › Pharmacology › Pharmaceutical industry and healthcare
  • Social Sciences › Safety Research › Academic integrity and plagiarism
  • Social Sciences › Decision Sciences › Information Systems and Management › Academic Publishing and Open Access
Keywords
ghost authorship, authorship criteria, pharmaceutical industry, acknowledgment of contributors, research transparency
MeSH terms
Authorship, Humans, Publishing, Scientific Misconduct, Randomized Controlled Trials as Topic, Biomedical Research

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