periorbital hyperpigmentation. -
Conditions
Interventions
Intervention 1: Intervention group 1 : Cases will be treated with microneedling therapy and use of local 10% trichloroacetic acid solution until frost formation , 3 sessions with a month intervals be
Treatment - Devices
Intervention group 1 : Cases will be treated with microneedling therapy and use of local 10% trichloroacetic acid solution until frost formation , 3 sessions with a month intervals between them. Due
Control group : The control group will be treated with fractional laser 3 sessions with a month intervals between them.
Sponsors
Vice chancellor for research , Iran University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
28 Years to 62 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: Ages from 28 to 63; Skin typesfrom 2 to 4 exclusion criteria: Absence of fallow up by patients and not satisfied to continue; Complications such as allergy to topical agent
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Preorbital hyperpigmentation. Timepoint: 0, 1 and 2 months during treatment . And 3 and 6 months after treatment. Method of measurement: Intensity of the darkening of the skin around the eyes compared to other areas of the face with visio face device. | — |
Secondary
| Measure | Time frame |
|---|---|
| Satisfaction amount. Timepoint: after completion of treatment. Method of measurement: Comparison of reduction preorbital hyperpigmentation by patient , before and after treatment According to schedule ( score 0 to 10 ).;Response to treatment According to the patient. Timepoint: after completion of treatment. Method of measurement: The percentage and score of the patient to treatment ( 0 to 100% ). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMahba Azizi
Iran University Of Medical Sciences
Outcome results
None listed