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Exploring differences in adverse symptom event grading thresholds between clinicians and patients in the clinical trial setting

PURPOSE: Symptomatic adverse event (AE) monitoring is essential in cancer clinical trials to assess patient safety, as well as inform decisions related to treatment and continued trial participation. As prior research has demonstrated that conventional concordance metrics (e.g., intraclass correlati...

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Detalhes bibliográficos
Publicado no:J Cancer Res Clin Oncol
Main Authors: Atkinson, Thomas M., Rogak, Lauren J., Heon, Narre, Ryan, Sean J., Shaw, Mary, Stark, Liora P., Bennett, Antonia V., Basch, Ethan, Li, Yuelin
Formato: Artigo
Idioma:Inglês
Publicado em: 2017
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5354957/
https://ncbi.nlm.nih.gov/pubmed/28093637
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00432-016-2335-9
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