Reporting Clinical End Points and Safety Events in an Acute Coronary Syndrome Trial: Results With Integrated Collection

BACKGROUND: End points and adverse events (AEs) are collected separately in clinical trials, yet regulatory requirements for serious AE reporting vary across regions, so classifying end points according to seriousness criteria can be useful in global trials. METHODS AND RESULTS: In the Apixaban for...

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Detalhes bibliográficos
Publicado no:J Am Heart Assoc
Main Authors: Guimarães, Patrícia O., Lopes, Renato D., Stevens, Susanna R., Zimerman, André, Wruck, Lisa, James, Stefan K., Haque, Ghazala, Giraldez, Roberto Rocha C. V., Alexander, John H., Alexander, Karen P.
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2017
Assuntos:
Original Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5533035/
https://ncbi.nlm.nih.gov/pubmed/28438739
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/JAHA.117.005490
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