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Discrepancies in the results reported for multiple sclerosis clinical trials: A comparison between ClinicalTrials.gov and peer-reviewed journals.

Rivero de Aguilar Pensado, Alejandro; Pérez-Ríos, Mónica; Mascareñas-García, Marta; Ruano-Raviña, Alberto; Ross, Joseph S; CASAL ACCION, BEATRIZ; Varela Lema, Leonor
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URI: http://hdl.handle.net/20.500.11940/22047
PMID: 39189062
DOI: 10.1177/13524585241273089
ISSN: 1352-4585
ESSN: 1477-0970
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Mult Scler . 2024 Oct;30(11-12):1514-1524 (466.6Kb)
Fecha de publicación
2024
Título de revista
Multiple sclerosis (Houndmills, Basingstoke, England)
 
MULTIPLE SCLEROSIS JOURNAL
 
Tipo de contenido
Artigo
DeCS
esclerosis | esclerosis múltiple
MeSH
Multiple Sclerosis | Publications | Safety | Bias | Sclerosis
Resumen
[EN] We aimed to compare the results of phase III and IV clinical trials examining drugs to treat multiple sclerosis (MS) registered at ClinicalTrials.gov to those published in peer-reviewed journals. After identifying trials registered at ClinicalTrials.gov, consecutive searches were conducted in PubMed, EMBASE and Google Scholar for matching publications. Information regarding participants and efficacy and safety results was extracted and compared. The degree of consistency was classified as 'concordant', 'discrepant' or 'not comparable'. The Kaplan-Meier method was used to model time to reporting. In total, 65 trials were appraised. The median time from completion to reporting was shorter for ClinicalTrials.gov (16.4 vs 27.3 months; p = 0.010). Information availability was generally higher in journals except for serious adverse events (SAEs) (86.2% vs 100.0%, p = 0.029) and their description (78.2% vs 100.0%, p < 0.001). However, 45 trials had at least one reporting discrepancy (69.2%). Three studies omitted one or more primary outcomes in the matching journal publication. Regarding safety results, the lowest consistencies were found for causes of death (60.0%) and description of SAEs (27.9%). Consulting both ClinicalTrials.gov and journals increases the accessibility to MS clinical trial results. Some data were frequently missing or disagreed between sources, raising concerns about transparency and generalizability of results.

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