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Vitiligo International Task force for an Agreed List of core data (VITAL): study protocol of a vitiligo core outcome set (COS) and contextual factors for clinical trials, registries, and clinical practice

BACKGROUND: There is a lack of consensus related to the collection of standardized data for individuals with vitiligo enrolled in clinical trials and registries as well as those seen in clinical practice which causes difficulty in accurately interpreting, comparing, and pooling of data. Several year...

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Detalles Bibliográficos
Autores principales: van Geel, Nanja, Hamzavi, Iltefat H., Pandya, Amit G., Wolkerstorfer, Albert, Seneschal, Julien, Garg, Amit, Spuls, Phyllis, Terwee, Caroline B., Mallett, Sue, Speeckaert, Reinhart, Meurant, Jean Marie, Eleftheriadou, Viktoria, Ezzedine, Khaled
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9308182/
https://www.ncbi.nlm.nih.gov/pubmed/35871019
http://dx.doi.org/10.1186/s13063-022-06497-1