None listed
Conditions
Interventions
Medical Device : A randomized, non-blind clinical study selected two or more, six or less circular alopecia lesions of similar shape and size, with one as the control group and the remaining as the ex
Sponsors
The Catholic University of Korea, St. Vincent's Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: (1) Children over 4 years of age, under 19 years of age (2) Patients with alopecia areata with at least two or six clinically confirmed lesions (3) Alopecia areata patients with less than 25% of all scalp involvement (4) Patients who have voluntarily agreed to participate in the study after being fully informed about the purpose and method of the study.
Exclusion criteria
Exclusion criteria: 1) Patients under 4 years old, 19 years old (2) patients with ophiasis, alopecia totalis, and alopecia universalis (3) patients with alopecia areata with seven or more lesions (4) Alopecia areata patients with scalp involvement of 25% or more (5) Patients who do not want themselves or their legal representatives or refuse to make a consent form (6) Patients who have received or are currently receiving systemic corticosteroids in the last month. (7) Person who is considered unsuitable for examination by judgment of other examination manager
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Hair regrowth | — |
Secondary
| Measure | Time frame |
|---|---|
| saftey | — |
Countries
Korea, Republic of
Contacts
Public ContactJihae Lee
The Catholic University of Korea
Outcome results
None listed