None listed
Conditions
Interventions
Medical Device : In the random selection method of the test group and the control group, in the case of rosacea patients, each side on the face of the subject is assigned, and in the case of nevus fla
Sponsors
Yonsei University Health System, Severance Hospital
Yonsei University Yongin Severance Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Adults aged 19-65 2) Individuals with cutaneous vascular lesions (rosacea, nevus flammeus) 3) Individuals who understands the purpose and methods of this trial 4) Individuals who can regularly visit our hospital 5) Individuals who agrees to avoid any other dermatologic therapies other than our treatment material
Exclusion criteria
Exclusion criteria: 1) Whom denies to participate 2) Pregnant women, breast feeding women 3) Subjects judged to be unsuitable by the person in charge of the clinical trial for the following conditions ? In case of infectious or inflammatory skin disease at the treatment site ? In case of pigmented skin diseases such as spots at the treatment site ? In case of keloid or collagen or elastic fiber disease ? In case of chronic wasting disease (asthma, diabetes, etc.) ? When there is a risk of bleeding by taking an anticoagulant ? In case of an autoimmune disease ? Person with psychiatric problems ? Person with acute illness 4) Other cases when it is difficult to conduct the clinical (ex. illiteracy, foreigners)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 5-point scale Global Aesthetic Improvement Scale (GAIS) evaluated based on clinical photos | — |
Secondary
| Measure | Time frame |
|---|---|
| Mark-vu, Mexameter, subjective improvement graded by participants | — |
Countries
Korea, Republic of
Contacts
Public ContactSujin Park
Yonsei University Health System, Severance Hospital
Outcome results
None listed