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Potential of patient-reported outcomes as nonprimary endpoints in clinical trials

BACKGROUND: The purpose of this research was to fully explore the impact of endpoint type (primary vs. nonprimary) on decisions related to patient-reported outcome (PRO) labeling claims supported by PRO measures and to determine if nonprimary PRO endpoints are being fully optimized. This review exam...

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Autori principali: Gnanasakthy, Ari, Lewis, Sandra, Clark, Marci, Mordin, Margaret, DeMuro, Carla
Natura: Artigo
Lingua:Inglês
Pubblicazione: BioMed Central 2013
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3667032/
https://ncbi.nlm.nih.gov/pubmed/23675876
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1477-7525-11-83
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