Stomatitis
Conditions
Interventions
This is a two-arm, double-blind, randomized controlled clinical trial. Participants were distributed according to a random sequence generated by the Excel program. Group intervention: 20 patients unde
D12.776.256.159.750
Sponsors
Universidade Federal de Juiz de Fora
Hospital Universitário da Universidade Federal de Juiz de Fora
Eligibility
Age
12 Years to No maximum
Inclusion criteria
Inclusion criteria: Age over 12 years old; both genders; patients who have not started the conditioning phase
Exclusion criteria
Exclusion criteria: Patients who are allergic to milk proteins; lactose intolerants; suspension of oral nutrition during treatment; death occurring during the data collection period
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Expected outcome 1: We anticipated finding a higher incidence of oral mucositis in the control group, as assessed by the World Health Organization oral toxicity scale.;Outcome found 1: The control group showed a higher incidence of oral mucositis (65%) compared to the intervention group (40%), as assessed by the World Health Organization oral toxicity scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| Expected outcome 2: We expected to find a higher degree of oral mucositis severity (grade 3 or more, according to the World Health Organization scale) in the control group patients.;Outcome found 2: The control group exhibited a 30% incidence of severe oral mucositis, whereas the intervention group showed a 10% incidence. | — |
Countries
Brazil
Contacts
Public ContactAbrahao Hallack Neto
Hospital Universitário da Universidade Federal de Juiz de Fora
Outcome results
None listed