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Are investigators’ access to trial data and rights to publish restricted and are potential trial participants informed about this? A comparison of trial protocols and informed consent materials

OBJECTIVES: To determine to which degree industry partners in randomised clinical trials own the data and can constrain publication rights of academic investigators. METHODS: Cohort study of trial protocols, publication agreements and other documents obtained through Freedom of Information requests,...

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Detalles Bibliográficos
Autores principales: Paludan-Müller, Asger S., Ogden, Michelle C., Marquardsen, Mikkel, Jørgensen, Karsten J., Gøtzsche, Peter C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8403412/
https://www.ncbi.nlm.nih.gov/pubmed/34454496
http://dx.doi.org/10.1186/s12910-021-00681-9

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