Cellulite. Localized adiposity
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Female patients older than ?? years old Confirm her cellulite by dermatologist
Exclusion criteria
Exclusion criteria: Pregnant and breastfeeding women History of thromboembolic events, diabetes mellitus, immunosuppression, kidney and liver failure, severe respiratory insufficiency, uncontrolled hypertension, co-existent febrile illness, gas gangrene, Having received aesthetic treatments in the gluteofemoral region in past six months Unwillingness to participate in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Severity of cellulite. Timepoint: At the beginning of the study and 8 weeks after the start of treatment. Method of measurement: Cellulite severity scale (CSS). | — |
Secondary
| Measure | Time frame |
|---|---|
| Quality of life. Timepoint: At the beginning of the study and 8 weeks after the start of treatment. Method of measurement: Dermatology Life Quality Index. | — |
Countries
Iran (Islamic Republic of)
Contacts
Shiraz University of Medical Sciences