Women
Conditions
Interventions
This is a randomized clinical trial on both thighs. A total of 144 volunteers, 72 men and 72 women, who meet the eligibility criteria, will be allocated into 12 groups: White men between 18 and 39 yea
E02.594.540
Sponsors
Universidade Federal de São Carlos
Universidade Federal de São Carlos
Eligibility
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: White, brown and black men and women. Body mass index (BMI) between 18.5 and 29.9 kg/m2. Skin fold in the vastus medialis area measuring up to 25 mm
Exclusion criteria
Exclusion criteria: Hypersensitivity to OCA-IPQ, such as redness and itching; skin lesions in the vastus medialis region such as open wounds; tattoos; history of skin cancer; cognitive difficulty reporting thermal sensation; pacemaker
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Applying OCA-CPE is expected to increase the light penetration into skin;Applying sonophoresis OCA-CPE is expected to increase the light penetration into skin, compared to the application of OCA-CPE | — |
Secondary
| Measure | Time frame |
|---|---|
| Compare data of light penetration into the skin of men and women with different age groups and skin color types | — |
Countries
Brazil
Contacts
Public ContactOtávio Dutra
Universidade Federal de São Carlos
Outcome results
None listed