Silva-Sperb, Amanda Souza http://orcid.org/0000-0002-8650-1003
Moraes, Helena Abadie
de Moura, Bruna Concheski
Alves, Bruna Cherubini
Bruch-Bertani, Juliana Paula
Azevedo, Vittoria Zambon
Dall’Alba, Valesca
Funding for this research was provided by:
Coordination for the Improvement of Higher Education Personnel
Research and Events Fund from the Hospital de Clínicas de Porto Alegre (15-0438)
National Council for Scientific and Technological Development (1/2016)
Article History
Received: 3 May 2019
Accepted: 24 August 2019
First Online: 10 October 2019
Ethics approval and consent to participate
: This research is approved by the Ethics Committee of Hospital de Clínicas de Porto Alegre, registered under numbers 16–0438, 17–0406, and 19–0289, and it is also registered at ClinicalTrials.gov under the identifier NCT03467282. In the possibility of any protocol change, this will be done through an amendment to this same approved project. Written informed consent will be obtained from all patients to be included in this clinical trial by the main researchers. In the informed consent is the patient’s agreement to allow the storage of their biological material (blood/feces) for future analysis.
: Not applicable.
: The authors declare that they have no competing interests.