acne. Acne vulgaris
Conditions
Interventions
Intervention 1: first intervention group: Adapalen 0.1% (najo company) was used on half of the face 3 times a week for 3 months and at the end of the first, second and third months of the beginning of
Sponsors
Esfahan University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
15 Years to 35 Years
Inclusion criteria
Inclusion criteria: prefer laser therapy no acne scar being non- pregnant and non-breast feeding Individual consent to participate in the study having no treatment with any systemic or local antibiotics in last 2 weeks not receiving systemic steroid and retinoid in the last 6 months. no sensitivity to laser Lack of history of hypertrophic and colloid scar formation Women 15-35 years old
Exclusion criteria
Exclusion criteria: allergic reaction to benzoyl peroxide allergic reaction to adapalene withdrawing from study using of other treatment for AV at the same time
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Acne Severity Index. Timepoint: Befor and 1, 2, 3 months after initiation and 1 month after the last visit. Method of measurement: Calculating corresponding formula based on the number of injuries. | — |
Secondary
| Measure | Time frame |
|---|---|
| Acne Global Severity Scale. Timepoint: Before, 1,2,3 month after treatment and 1 month after final treatment. Method of measurement: Calculating corresponding formula based on the number of injuries. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAtefeh Shajari
Esfahan University of Medical Sciences
Outcome results
None listed