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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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Bibliographische Detailangaben
Veröffentlicht in:Clin Trials
Hauptverfasser: 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
Format: Artigo
Sprache:Inglês
Veröffentlicht: 2017
Schlagworte:
Online Zugang: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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