Writing a research protocol in pediatric oncology

Autores

  • Maryelle Moreira Lima Gamboa HCPA
  • Lauro Gregianin Hospital de Clínicas de Porto Alegre

Palavras-chave:

Protocolo de Pesquisa, Oncologia Pediátrica, Termo de Consentimento Livre e Esclarecido

Resumo

Children are considered an especially vulnerable population in a clinical trial. Specific regulations of research in pediatrics are focused upon protection from potential risks. Clinical trials in oncology have become an important step to the researchers to discover new drugs, new combinations of known drugs and new methodologies. The aim of this manuscript is to help the starter researchers to elaborate pediatrics oncology protocols for clinical trials. This guide describes the relevant aspects before writing a research protocol and a template of research protocol. Moreover, it shows the importance of a well-designed research protocol and its attachments - informed consent and assent forms – in a pediatric oncology study.

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Biografia do Autor

Maryelle Moreira Lima Gamboa, HCPA

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Publicado

2013-07-23

Como Citar

1.
Gamboa MML, Gregianin L. Writing a research protocol in pediatric oncology. Clin Biomed Res [Internet]. 23º de julho de 2013 [citado 1º de outubro de 2022];33(2). Disponível em: https://seer.ufrgs.br/index.php/hcpa/article/view/35786

Edição

Seção

Seção de Bioética