Acne vulgaris. Acne vulgaris
Conditions
Interventions
Intervention 1: First intervention group: Argon plasma. In this method, an argon plasma device manufactured by Danesh Banyan Engineering Plasma Technology Co., Ltd. is used to process acne. In this me
Sponsors
Tehran University of Medical Sciences
Shahid Beheshti University
Eligibility
Sex/Gender
Female
Age
16 Years to 55 Years
Inclusion criteria
Inclusion criteria: Phototype I _ VI Fitzpatrick The number of pores = 10 in each half of the face Inflammatory lesions (papules and pustules) = 50 in the whole face and = 10 in each half of the face Non-inflammatory lesions (open and closed comedones) = 50 in the whole face and = 10 in each half of the face Maximum 4 nodules with a diameter = 1 cm in the whole face Atrophic scars = 50 in the whole face and of any type (needle, box, rolling) = 5 in each half of the face Symmetrical distribution of lesions on both sides of the face Age 16 to 55 years old Gender: Female
Exclusion criteria
Exclusion criteria: Acne conglobata Acne fulminans Secondary acne (drugs and hormones) Nodulocystic acne Acne requires systemic treatment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pour and their size in each visit. Timepoint: Variables are measured before, immediately after, one week, two weeks, three weeks, four weeks and eight weeks after the start of treatment. Method of measurement: They are measured and recorded by the SKIN SCANNER device.;Scars and their size. Timepoint: Variables are measured before, immediately after, one week, two weeks, three weeks, four weeks and eight weeks after the start of treatment. Method of measurement: They are measured and recorded by the SKIN SCANNER device.;Inflammatory and non-inflammatory acne lesions. Timepoint: Variables are measured before, immediately after, one week, two weeks, three weeks, four weeks and eight weeks after the start of treatment. Method of measurement: They are measured and recorded by the SKIN SCANNER device.;Acne severity. Timepoint: Variables are measured before, immediately after, one week, two weeks, three weeks, four weeks and eight weeks after the start of treatment. Method of measurement: They are measured and recorded by the SKIN SCANNER device.;Examination of skin roughness. Timepoint: Variables are measured before, immediately after, one week, two weeks, three weeks, four weeks and eight weeks after the start of treatment. Method of measurement: They are measured and recorded by the SKIN SCANNER device.;Skin biometric parameters. Timepoint: Variables are measured before, immediately after, one week, two weeks, three weeks, four weeks and eight weeks after the start of treatment. Method of measurement: This item is quantitatively measured and reported by CUTOMETER and MPA 9 devices. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMohammadreza Khani
Laser and Plasma Research Institute/ Shahid Beheshti University
Outcome results
None listed