Hair loss. Nonscarring hair loss, unspecified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Male or female aged 18-55 years Diffuse and scattered hair loss (Count at least 300 hairs in a combing test over three days) General health Voluntary participation and signing written informed consent
Exclusion criteria
Exclusion criteria: Men and women with androgenetic pattern hair loss (Hamilton grade 3 and above in men and Ludwig grade 2 and above in women) Pregnancy or breastfeeding Clinical hyperandrogenism in the form of pronounced hirsutism and menstrual disorders in women Chronic active scalp disease other than hair loss Using any prescribed drug or Over The Counter(OTC) for hair loss within the past 3 months
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Hair lost Changes, based on Global photographic review. Timepoint: Before intervention, 6 and 12 weeks after the intervention. 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 12 weeks after the intervention. Method of measurement: Trichoscopy by Fotofinder.;Terminal hairs count. Timepoint: Before intervention, 8 and 12 weeks after the intervention. Method of measurement: Trichoscopy by Fotofinder. | — |
Countries
Iran (Islamic Republic of)
Contacts
Tehran University of Medical Sciences