hair loss. Nonscarring hair loss, unspecified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Male aged 18-50 years General health Voluntary participation and signing written informed consent Hair Loss Status II, III, IV Based on Norwood Scale
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 People with allergies to tonic and shampoo ingredients Any severe weight loss or strict diet therapy during the study
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| Hair count changes. Timepoint: Before intervention, 6 and 12 weeks after the start of use. Method of measurement: Trichoscopy By Fotofinder.;Changes in percentage of anagen to telogen. Timepoint: Before intervention, 6 and 12 weeks the start of use. Method of measurement: Trichoscopy by Fotofinder. | — |
Primary
| Measure | Time frame |
|---|---|
| Hair lost Changes, based on Global photographic review. Timepoint: Before intervention, 6 and 12 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 . | — |
Countries
Iran (Islamic Republic of)
Contacts
Tehran University of Medical Sciences