skin rejuvenation. Other specified disorders of the skin and subcutaneous tissue
Conditions
Interventions
Intervention 1: Intervention group:one of the people's hands are randomly selected for plasma processing and another laser (a group of 25 CO2 fractional lasers - a group of 25 Nd: YAG lasers - a group
Sponsors
Shahid Beheshti University of Medical Sciences
Shahid Beheshti University
Eligibility
Sex/Gender
Female
Age
35 Years to 70 Years
Inclusion criteria
Inclusion criteria: in a certain age category female mild and moderate photodamaged no exclusion criteria Satisfaction to enter the study
Exclusion criteria
Exclusion criteria: Age>70 and <35 years old The history of dermatological diseases Pregnancy and lactation History of Skin rejuvenation in the last 6 months Male gender Smokers and/or alcoholics Lack of satisfaction to enter the study Active malignancy in the treated area Active infection in the treated area
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Skin elasticity. Timepoint: before treatment_before each session_1month after the last session _3month after the last session. Method of measurement: resonance running time_reviscometer.;Rhytids improvement. Timepoint: before treatment_before each session_1month after the last session _3month after the last session. Method of measurement: reviscometer_mexameter_corneometer_tewameter_Percentage of improvement by comparing photos by a dermatologist_ Patient Satisfaction.;Solar lentigo improvement. Timepoint: before treatment_before each session_1month after the last session _3month after the last session. Method of measurement: reviscometer_mexameter_corneometer_tewameter_Percentage of improvement by comparing photos by a dermatologist_ Patient Satisfaction.;Patient satisfaction. Timepoint: before treatment_before each session_1month after the last session _3month after the last session. Method of measurement: percentage Patient satisfaction_ questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Side effects(pain-burning and stinging-erythem-edema-bulla-bleeding-crust formation-hypopigmentation-hyperpigmentation-scar-atrophy). Timepoint: one week after each treatment session. Method of measurement: patient evaluation with questionnaire-dermatologist evaluation.;Side effects lasting. Timepoint: until one week after each treatment. Method of measurement: by day. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactShima Babosalam- Katayoon Hadian
Shahid Beheshti University
Outcome results
None listed