Working towards consensus on methods used to elicit participant-reported safety data in uncomplicated malaria clinical drug studies: a Delphi technique study

BACKGROUND: Eliciting adverse event (AE) and non-study medication data reports from clinical research participants is integral to evaluating drug safety. However, using different methods to question participants yields inconsistent results, compromising the interpretation, comparison and pooling of...

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Detalles Bibliográficos
Autores principales: Mandimika, Nyaradzo, Barnes, Karen I., Chandler, Clare I. R., Pace, Cheryl, Allen, Elizabeth N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5273807/
https://www.ncbi.nlm.nih.gov/pubmed/28129765
http://dx.doi.org/10.1186/s12936-017-1699-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5273807/
https://www.ncbi.nlm.nih.gov/pubmed/28129765
http://dx.doi.org/10.1186/s12936-017-1699-x

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