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Effect of PRP on male pattern hair loss

Assessment of autologous Platelet-Rich Plasma Injections in the Treatment of male pattern Androgenetic Alopecia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016021526563N1
Enrollment
20
Registered
2016-05-29
Start date
2015-07-23
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

Male androgenetic alopecia. Androgenic alopecia

Interventions

injection of Platelet-Rich Plasma (PRP) 3 times in 4 weeks..
Treatment - Other
injection of Platelet-Rich Plasma (PRP) 3 times in 4 weeks.

Sponsors

Vice chancellor for research of Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
28 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients include males with male pattern androgenetic alopecia who had acquiescence for participation in this study and their baldness is grade 3v to 5 according to Hamilton-Norwood scaling system. Exclusion criteria: using minoxidil or finasteride in the last 6 months; using any other systemic or topical supplementary drugs for hair growth stimulation in the last 6 months; using drugs that can induce hair loss (eg. Retinoids, heavy metals, antithyroids, anticonvulsants, betablockers and …); specific diseases like thyroid disease, collagen vascular disease …; positive history for any kind of cancer or skin cancer and chemotherapy; any other kind of alopecia ( scaring alopecia, alopecia areata, …); steroid therapy; coagulation disorders, acquisition of aspirin, ticlopidine or other anticoagulative drugs; dialysis patients and platelet disorders (thrombocytopenia); smoker and alcoholic persons and malnutrition; and anytime patient wants to leave the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Hair loss improvement and stimulation of hair growth. Timepoint: Measurement on weeks 0, 4, 8, 12 and 3 months after last injection. Method of measurement: Average hair diameter and hair count in unit surface.

Secondary

MeasureTime frame
Side effects. Timepoint: At the end of treatment (3 months after last injection). Method of measurement: Effectiveness and side effects include local and systemic reactions according to patients and investigator observations.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Mohammad Javad Yazdanpanah

Mashhad University of Medical Sciences

yazdanpanahmj@mums.ac.ir+98 51 3801 2493

Outcome results

None listed

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