Radiodermatitis
Conditions
Interventions
This is a two-arm, double-blind, randomized controlled clinical study. Patients diagnosed with radiodermatitis will be divided into two groups. Experimental group: 40 patients will receive treatment w
E02.594.540
Sponsors
Universidade Federal de Santa Maria
Universidade Federal de Santa Maria
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Individuals of both sexes; cancer and ending with radiotherapy; I tend to develop radiodermite in any gray
Exclusion criteria
Exclusion criteria: Minors under 18 years of age; metastase na pele; concomitant chemotherapy; infection in the region to be treated; história de doenças de pele ou autoimmunes; history of photosensitivity; inability to answer questions
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected that the intervention group will have a faster recovery from damaged skin due to radiodermite, when compared to the control group. The degree of radiodermite will be evaluated by the Radiation Therapy Oncology Group scale | — |
Secondary
| Measure | Time frame |
|---|---|
| Expect to promote better quality of life specific dermatologically endorsed questionnaire Skindex-16 | — |
Countries
Brazil
Contacts
Public ContactHedioneia Pivetta
Universidade Federal de Santa Maria
Outcome results
None listed