Ulcer
Conditions
Interventions
This is a phase 1 controlled clinical trial. A total of 20 people who meet the eligibility criteria will be no probabilistically allocated to either the intervention group or the control group. The ex
Sponsors
Universidade Estadual da Paraíba
Hospital Universitário Alcides Carneiros
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Individuals over 18 years old. Both sexes. With diabetic ulcers. Grade 0 or 1 classification according to the University of Texas Grading System. 1 to 10 cm2 lesion size. Ulcers can be located in the forefoot, midfoot or lower third of the leg. Availability to go to the service once a week
Exclusion criteria
Exclusion criteria: Infected ulcers. Intolerance to the odor of the dressing. Allergy to the research product used. Lack of continuity of treatment at home. Pregnant and lactating women
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The presentation of the expected outcome is the reduction of the wound area, verified through horizontal and vertical measurements in the largest diameter of the wound, the presentation of the parameters will be through percentage reductions, expecting that there will be a significant reduction of the wound after 3 months of treatment. treatment. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes are not expected. | — |
Countries
Brazil
Contacts
Public ContactMarcus Lia Fook
Universidade Federal de Campina Grande
Outcome results
None listed