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Evaluation the effect of blood platelet on androgenic hair loss

Comparison the effect of plasma rich platelet with finastride and placebo on androgenic hair loss

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014062918210N2
Enrollment
120
Registered
2014-09-17
Start date
2013-01-31
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Androgenetic alopecia. Androgenetic alopecia

Interventions

Intervention 1: Interventional group:plasma rich platelet,is uptaken from their blood after sentrifuge. Intervention 2: Control group1:take 1 miligram finastride daily. Intervention 3: Control group2:
Treatment - Other
Treatment - Drugs
Placebo
Interventional group:plasma rich platelet,is uptaken from their blood after sentrifuge
Control group1:take 1 miligram finastride daily
Control group2:apply placebo once aday on their head,placebo composed of 25% alcohol and 75% N/S

Sponsors

Vice Chancellor of Iran university of Medical science-Research committee
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
20 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: androgenic alopecia Hamilton grade 2 and 3; 20-35 years old men;normal laboratory tests of TSH, CBC AND ferritin ; do not use oral finastride or topical minoxidil for the last 3 months.Exclusion criteria:another systemic or topical disease on the scalp;use of telogen effluvium drugs;nutritional disease;scarring alopecia)

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Androgenetic alopecia. Timepoint: 3 months and 6months later. Method of measurement: Photography.

Secondary

MeasureTime frame
Hair growing. Timepoint: 3months and 6 months later. Method of measurement: Photography.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Elham Behrangi

Iran University of Medical Science

behrangi.e@iums.ac.ir+98 21 6650 2040

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026