A study to evaluate the safety and effectiveness of a micro coring device for the treatment of scars.
The study subject population will consist to up to 30 subjects who meet the inclusion/exclusion criteria. All subjects will be monitored for a period of 6 months post last treatment. An study results will be assessed on the following: * POSAS - Patient Observer Scar Assessment * ASAS - Acne Scar Severity Scale * Subject Satisfaction Scale
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
30
Micro coring skin removal with automated coring device
Miami Dermatology & Laser Institute
Miami, Florida, United States
RECRUITINGAssess level of aesthetic improvement using POSAS scale 6 months post last treatment
Assessing the improvement in the aesthetic appearance of the subject based on the POSAS scale comparing baseline to 6 months post last treatment. Parameters of vascularity, pigmentation, thickness, relief, and pliability, range from 1 to 10. normal skin =1; worst scar imaginable =10.
Time frame: 6 months post last treatment
Assess level of aesthetic improvement using ASAS scale 6 months post last treatment
Assessing the improvement in the aesthetic appearance of the subject based on the Acne Scar scale comparing baseline to 6 months post last treatment. Grades range 0-4. Clear =0; Very Mild=1; Mild= 2; Moderate= 3; Severe= 4
Time frame: 6 months post last treatment
Assess safety profile by recording all adverse events reported during study
Adverse events will be recorded throughout the study
Time frame: 6 months post last treatment
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