None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: ? Alopecia areata volunteers with a lesion of 3 cm or more in the long diameter within 1 year on the scalp ? A person who voluntarily decides to participate after hearing the detailed explanation of this clinical trial and agrees in writing to abide by the precautions ? Men and women over the age of 20 ? Volunteers available for follow-up during the trial period
Exclusion criteria
Exclusion criteria: ? Those who have not observed hair regrowth even after treatment (oral, topical, injection treatment of the lesion subject to study) for more than 6 months after the occurrence of bald spots ? Those with clear hair regrowth in the alopecia lesion ? Those who show ophiasis pattern ? Those who have received drug treatment (oral, topical, injection) for alopecia areata within one month ? Those with other diseases of the scalp or hair ? Women who are pregnant or lactating ? Those with cold intolerance or immune diseases other than alopecia areata ? Those with psychiatric illness ? Those judged by the principal investigator to be ineligible as a study subject
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| improvement rate of alopecia lesion | — |
Secondary
| Measure | Time frame |
|---|---|
| preference for cryotherapy | — |
Countries
Korea, Republic of
Contacts
Seoul National University Hospital