Evaluation of different recall periods for the US National Cancer Institute’s Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE)

AIMS: The U.S. National Cancer Institute recently developed the Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE). PRO-CTCAE is a library of questions for clinical trial participants to self-report symptomatic adverse events (e.g., nausea). The objec...

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Publicado en:Clin Trials
Main Authors: Mendoza, Tito R., Dueck, Amylou C., Bennett, Antonia V., Mitchell, Sandra A., Reeve, Bryce B., Atkinson, Thomas M., Li, Yuelin, Castro, Kathleen M., Denicoff, Andrea, Rogak, Lauren J., Piekarz, Richard L., Cleeland, Charles S., Sloan, Jeff, Schrag, Deborah, Basch, Ethan
Formato: Artigo
Idioma:Inglês
Publicado: 2017
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Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC5448293/
https://ncbi.nlm.nih.gov/pubmed/28545337
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/1740774517698645
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