Diabetic foot
Conditions
Interventions
A double-blind randomized clinical trial. The sample will consist of 66 participants, aged between 18 and 75 years, with diabetic foot wounds, who will be divided into 2 groups of 33 participants, wit
the control group of 33 participants (GII) will follow the standard treatment mentioned above, but without ILIB irradiation. Randomization will be performed by a person independent of the study team t
E02.594
Sponsors
Departamento de Fisioterapia da Universidade Federal do Ceará
Departamento de Fisioterapia da Universidade Federal do Ceará
Eligibility
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: diabetic volunteers of both genders; aged between 18 and 75 years; with non-infected diabetic foot wounds
Exclusion criteria
Exclusion criteria: volunteers with infected wounds; with cognitive deficits; carriers of autoimmune diseases; bilateral upper limb amputees; carriers of other skin diseases in addition to diabetic wounds
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate tissue cation, determined by measuring with a caliper in centimeters, comparing the control group with the intervention group;Evaluate a possible reduction in the percentage of blood glucose, determined by laboratory blood analysis in numbers, examination carried out pre and post-intervention | — |
Secondary
| Measure | Time frame |
|---|---|
| Assess whether there will be an improvement in oxidative stress variables, determined by laboratory blood analysis in numbers, examination performed pre and post-intervention;Assess whether there will be an improvement in the functionality of volunteers, determined by the quality of life measurement questionnaire - SF-36 through its score | — |
Countries
Brazil
Contacts
Public ContactMarcos da Silva
Departamento de Fisioterapia da Universidade Federal do Ceará
Outcome results
None listed