Poor registration and publication practices in clinical trials of targeted therapeutics for endocrine and metabolic

Maja Pavić1, Ružica Tokalić2, Ana Marušić3

  • 1Department of Dermatovenerology, University Hospital of Split, Šoltanska 1, Split 21 000, Croatia.

PubMed
Abstract

Insights

Reporting of targeted therapeutics clinical trials for endocrine and metabolic disorders is incomplete and inconsistent. Mandatory data items are frequently missing in registries and publications, raising concerns about trial integrity.

Area of Science:

  • Endocrinology and Metabolism
  • Clinical Trial Methodology
  • Data Reporting Standards

Background:

  • Accurate and complete reporting of clinical trial data is crucial for evidence-based medicine.
  • Interventional trials for targeted therapeutics in endocrine and metabolic disorders require transparent data dissemination.
  • Existing regulations mandate comprehensive registration and publication of trial information.

Purpose of the Study:

  • To evaluate the completeness and consistency of data reporting in clinical trial registries and their corresponding publications.
  • To assess interventional trials focused on targeted therapeutics for endocrine and metabolic disorders.
  • To identify discrepancies between initial registry entries, final updates, and published findings.

Main Methods:

  • Systematic search of clinical trial registries (ClinicalTrials.gov, WHO ICTRP) for completed interventional trials from 2005 onwards.
  • Extraction and analysis of mandatory registration data items for completeness and concordance.
  • Comparison of initial registration data, final registration updates, and published journal articles.

Main Results:

  • Of 149 trials, 121 (81%) had publications. 67% of initial registrations and 77% of publications lacked mandatory data.
  • All trials showed changes between initial registration and final update, and 98% changed from initial registration to publication.
  • Common discrepancies involved 'Completion date', 'Key secondary outcomes', 'Date of first enrolment', 'Sample size', and 'Key inclusion and exclusion criteria'.

Conclusions:

  • Reporting completeness and consistency in registries and publications for targeted therapeutics trials are inadequate.
  • Significant changes and missing mandatory data items question the integrity and reliability of reported trial findings.
  • There is an urgent need for improved adherence to registration and reporting requirements in clinical research.

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