Stomatitis
Conditions
Interventions
This is an experimental study, called a randomized clinical trial, aimed at evaluating the efficacy of propolis spray in the treatment of radiotherapy-induced oral mucositis in patients with head and
patients undergoing radiotherapy with or without associated chemotherapy
patients over 18 years of age. Exclusion criteria: patients with metastasis
patients undergoing radiotherapy as palliative care
patients with allergies to propolis or any substance contained in the spray formula
patients unable to answer the questionnaires or in a serious condition that prevents them from participating in the study. Patient randomization will be simple, through a draw using opaque, sealed, an
Sponsors
Sociedade Pernambucana de Combate ao Câncer
Sociedade Pernambucana de Combate ao Câncer
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients with head and neck cancer; patients undergoing radiation therapy with or without associated chemotherapy; patients over 18 years of age, from both sexes
Exclusion criteria
Exclusion criteria: Patients with metastasis; latients undergoing radiotherapy as palliative care; patients with allergies to propolis or any substance contained in the spray formula; patients unable to complete the questionnaires or in a serious condition that prevents them from participating in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected that the use of the propolis spray will reduce the incidence and severity of oral mucositis, significantly improving the quality of life of patients undergoing radiotherapy. In addition, lower hospitalization rates and reduced analgesic use are anticipated, leading to decreased healthcare costs. The use of a natural, affordable, and low-cost product may enhance treatment adherence. The expected impact includes fewer clinical and social complications associated with the disease. Thus, this study may contribute to effective, safe, and sustainable therapeutic alternatives. | — |
Secondary
| Measure | Time frame |
|---|---|
| No secondary outcomes are expected | — |
Countries
Brazil
Contacts
Public ContactKatarina Pessôa
Universidade Federal de Pernambuco
Outcome results
None listed