None listed
Conditions
Interventions
Medical Device : Before laser treatment, 30mg of 500mL of anesthetic cream with 25mg (0.0125%) of ICG is applied to the face and sealed for 15 minutes. 785nm 600 picosecond laser with DOE mode consis
Sponsors
Hallym University Medical Center
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Those who voluntarily agree to participate in the clinical trial. 2. Healthy adults who are 19 and above. 3. Persons who are willing to comply with the clinical trial protocol. 4. Persons who agree to and are willing to visit during the follow up period. 5. Persons who have enlarged pores, wrinkles and pigmented lesions.
Exclusion criteria
Exclusion criteria: 1. Those who do not want to voluntarily participate or those who do are not willing to sign the agreement. 2. Those with facial infection, dermatitis, or rash. 3. Those with serious systemic disease or infection. 4.Those who are not able to participate in follow up or monitoring. 5. Any other person who, at the discretion of the examiner, judges of doctor. 6. Pregnant or lactating.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| First effective evaluation of treatment (Pigmentation, pore and wrinkle evaluation on a 10-point VAS scale utilizing 3D camera and A-one spectrophotometer) | — |
Secondary
| Measure | Time frame |
|---|---|
| The area fraction of collagen fibers (Area fraction evaluated with Image J) | — |
Countries
Korea, Republic of
Contacts
Public ContactDayeon Jung
Hallym University Medical Center
Outcome results
None listed