Stomatitis, Oral mucositis
Conditions
Interventions
This study, a randomized clinical trial of intervention, will be carried out into two groups:
Group 1 (study group)
This group will be composed by 60 patients with OM > 1 submitted to antimicrobial
Other
E02.186.500
E02.594.540
Sponsors
Universidade Federal de Pernambuco
Instituto de Medicina Integral Prof. Fernando Figueira
Hospital Universitário Oswaldo Cruz
Eligibility
Age
0 Years to 21 Years
Inclusion criteria
Inclusion criteria: Patients from zero to twenty-one years, both genders, diagnosed with malignancies undergoing quimiotherapy;Pediatric patients diagnosed with OM > 1 (WHO);Patients in accordance with the research by signing the informed consent.
Exclusion criteria
Exclusion criteria: Patients with malignancies in oral cavity; Patients incapable of complying with the treatment; Patients in a serious situation that prevents participation in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Clinical cure of the oral mucositis expressed by at least one point regretion on the World Health Organization (WHO) mucositis scale and pain absence registered on Children’s International Mucositis Evaluation Scale (ChIMES). | — |
Secondary
| Measure | Time frame |
|---|---|
| Secundary outcomes are not expected | — |
Countries
Brazil
Contacts
Public ContactVânia Silva
Universidade Federal de Pernambuco
Outcome results
None listed