Writing a research protocol in pediatric oncology

Authors

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

DOI:

https://doi.org/10.22491/2357-9730.35786

Keywords:

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

Abstract

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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Author Biography

Maryelle Moreira Lima Gamboa, HCPA

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Published

2013-07-23

How to Cite

1.
Gamboa MML, Gregianin L. Writing a research protocol in pediatric oncology. Clin Biomed Res [Internet]. 2013 Jul. 23 [cited 2025 Aug. 11];33(2). Available from: https://seer.ufrgs.br/index.php/hcpa/article/view/35786

Issue

Section

Bioethics

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