Clinical Research Directory

Inclusion Criteria: * Male or female adults aged 18 to 54 years with androgenetic alopecia diagnosed according to at least one of the following applicable classification systems: * Basic and Specific classification: basic type M1 or higher, C1 or higher, or U1 or higher, together with specific type V1 or higher or F1 or higher * Norwood-Hamilton classification: stage II or higher for male participants * Ludwig classification: stage I or higher for female participants * Participants willing to avoid special hair products, hair treatments, and other manipulation of the hair during the study period * Participants willing to maintain the same hairstyle and hair color as at the first study visit throughout the study period * Participants who understood the purpose of the study and voluntarily provided written informed consent Exclusion Criteria: * Serious acute renal or cardiac disease, or another chronic disease such as hypertension or diabetes, within the previous 6 months that could affect the study results * Pregnancy, breastfeeding, or plans to become pregnant within 6 months * Psychiatric disease * Infectious skin disease * Previous surgical treatment for hair loss, including hair transplantation or scalp reduction surgery * Use of oral dutasteride or finasteride within the previous 6 months * Use of topical hair growth products, hair tonics, or other products intended to promote hair growth within the previous month * Use within the previous month of steroids, cytotoxic agents, vasodilators, antihypertensive agents, anticonvulsants, beta-blockers, bronchodilators, diuretics, spironolactone, cimetidine, diazoxide, cyclosporine, or ketoconazole * Use of a topical corticosteroid on the scalp within the previous month * Severe seborrheic dermatitis, scalp psoriasis, scalp infection, or another scalp condition considered likely to interfere with application of the study product * A hair loss disorder other than androgenetic alopecia, including alopecia areata, telogen effluvium, or scarring alopecia * Nutritional deficiency caused by excessive dietary restriction, gastrectomy, or another condition, or use of nutritional supplements that could affect hair loss * Any other condition considered by the principal investigator to make the individual unsuitable for study participation