hair loss. Nonscarring hair loss, unspecified
Conditions
Interventions
Intervention group: Intervention group: Daily use of oral anti-hair loos capsules containing 5 mg of biotin, 1 mg of finasteride, 1 mg of minoxidil as active ingredients more over lactose monohydrate
Sponsors
Knowledge-based company of Janus
Eligibility
Sex/Gender
Male
Age
18 Years to 50 Years
Inclusion criteria
Inclusion criteria: Male aged 18-50 years General health Hair Loss Status II, III, IV Based on Norwood Scale Voluntary participation and signing written informed consent
Exclusion criteria
Exclusion criteria: Chronic active scalp disease other than hair loss Using any prescribed drug or OTC for hair loss within the past 3 months Documented sensitivity to formulation components Any severe weight loss or strict diet therapy during the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Hair lost Changes, based on Global photographic review. Timepoint: Before intervention, 8 and 16 weeks after the start of use. Method of measurement: One independent dermatologist will perform clinical assessments in a blinded fashion by scoring every photograph according to the Global photographic review scale . | — |
Secondary
| Measure | Time frame |
|---|---|
| Hair count changes. Timepoint: Before intervention, 8 and 16 weeks after the start of use. Method of measurement: Trichoscopy By Fotofinder. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAniseh Samadi
Tehran University of Medical Sciences
Outcome results
None listed