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May 31, 20260 citationsOpen Access

Primary Outcome Discrepancies Between Trial Registrations and Publications: Analysis of 46,365 Trials on ClinicalTrials.gov

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HFHayden Farquhar

Key Points

  • This research aims to quantify the prevalence of primary outcome discrepancies between clinical trial registrations and publications.
  • Analyzed 46,365 completed interventional trials posted on ClinicalTrials.gov (2015–2025)
  • Automated screening identified possible discrepancies in trial-publication pairs
  • Manual verification assessed the nature of discrepancies in selected pairs.
  • 59.4% of trials had at least one matched publication
  • Automated screening flagged 24.7% as possible discrepancies with only 4.9% confirmed as true discrepancies
  • Discrepancies were mostly minor modifications, not major outcome changes.

Abstract

Version 1.1 (2026-05-29): Corrected a typographical error in the author ORCID iD shown in the manuscript PDF (now 0009-0002-6226-440X). No changes to data, methods, results, or conclusions. This study quantifies the prevalence and predictors of primary outcome discrepancies between clinical trial registrations and publications at unprecedented scale, analysing all 46,365 completed interventional trials with posted results on ClinicalTrials.gov (2015–2025). Key Findings 59.4% of trials (27,555/46,365) were matched to at least one publication Automated screening flagged 24.7% (3,353/13,595) of confirmed trial-publication pairs as possible discrepancies Manual validation of 123 pairs found 6 true discrepancies (4.9%; 95% CI 1.6–8.9%) Discrepancies were predominantly minor modifications, not substantive outcome switching No association between primary outcome statistical significance and discrepancy flagging (21.0% vs 20.6%; p=0.745) Phase 1 trials had the highest automated flag rate (47.4%), Phase 4 the lowest (15.6%) Implications: Primary outcome discrepancies affect approximately 5% of clinical trials and are predominantly minor rather than substantive. Critically, discrepancy rates are not associated with result significance, suggesting that outcome switching is not systematically driven by unfavourable results at the population level. Automated screening can efficiently triage trial populations but lacks sensitivity for subtle discrepancies. Contents: Main manuscript (PDF and DOCX), supplementary materials (PDF), and high-resolution main figures (3 PNG).

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Cite This Study

Hayden Farquhar (2026) studied this question.

synapsesocial.com/papers/6a1bd2515783ba022b6fdcb4https://doi.org/10.5281/zenodo.20438101
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