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Authors
Gallassi, Andrea Donatti https://orcid.org/0000-0003-1852-485X
de Oliveira, André Wagner Carvalho https://orcid.org/0000-0001-8041-2133
Rodrigues, Larissa Alencar https://orcid.org/0000-0002-6469-4318
Nakano, Eduardo Yoshio https://orcid.org/0000-0002-9071-8512
Ruas, Pedro A. S. https://orcid.org/0000-0002-1310-2634
de La Mata, José Antonio Iturri https://orcid.org/0000-0002-6598-1861
Júnior, Ettore Ferrari https://orcid.org/0000-0002-2953-7878
de Andrade Gomes, Juliano https://orcid.org/0000-0001-5990-765X
Caroba, Mariana Emanuele Silva https://orcid.org/0000-0003-1194-1407
dos Santos Silva, Marianna Gabriella https://orcid.org/0000-0002-1484-3856
Vieira, Mariana G. Q. https://orcid.org/0000-0002-8274-7882
Reis, Julia G. G. R. https://orcid.org/0000-0002-1129-2163
Leite, Jade Luiza Moreira https://orcid.org/0000-0003-2487-0118
de Lima, Guilherme Henrique Alves https://orcid.org/0000-0001-8571-1351
Lima, Jonathan Morais https://orcid.org/0000-0002-0273-0635
Lima, Yasmim P. V. https://orcid.org/0000-0002-9782-9258
Ribas, Jorge A. A. https://orcid.org/0000-0002-4363-2011
das Chagas, Nathalia A. L. https://orcid.org/0000-0002-4980-6799
Magalhães, Mateus A. https://orcid.org/0000-0002-8465-4428
da Silva, Mateus F. https://orcid.org/0000-0001-7628-9267
Filev, Renato https://orcid.org/0000-0002-9238-0455
Malcher-Lopes, Renato https://orcid.org/0000-0002-4941-9908
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Article History
Accepted: 24 March 2024
First Online: 8 April 2024
Declarations
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: Faculty of Ceilândia Research Ethics Committee of the UnB approved this study (certificate number CAAE: 82559418.5.0000.8093/2018; available to consult at ). The National Health Surveillance Agency authorized the importation and storage of the substances—<i>Anvisa do Brasil</i> (AEP/n°005/2019).All procedures followed were in accordance with the ethical standards of the responsible committee on human experimentation (institutional and national) and with the Helsinki Declaration of 1975, as revised in 2000. Informed consent was obtained from all participants to be included in the study. The Clinical Trial Protocol was built according to the recommendations of the Standard Protocol Items: Recommendations for Interventional Trials (SPIRIT), and the preparation of the manuscript followed the guidelines of the Consolidated Standards of Reporting Trials (CONSORT), which establishes evidence-based recommendations for reporting clinical trials (CONSORT checklist available after the “References” section).
: All authors have participated in the study and approved this submission.
: The authors declare no competing interests.
