Skip to content

Placenta growth factors in the treatment of androgenetic alopecia

Clinical trial of safety and effectiveness of subcutaneous injection of placenta Growth factors in the treatment of androgenetic alopecia

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210612051545N4
Enrollment
30
Registered
2022-12-05
Start date
2022-12-01
Completion date
Unknown
Last updated
2023-02-07

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

Conditions

Androgenic alopecia. Androgenic alopecia

Interventions

Intervention 1: Intervention group: Subcutaneous injection of the solution containing growth factors obtained from the human placenta is performed in 15 patients with androgenic alopecia. Placental gr

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Patients with androgenetic alopecia Age 18 to 50 years Male Norwood-Hamilton grade II to V

Exclusion criteria

Exclusion criteria: Patients with two or more diagnoses of hair loss Treatment of hair loss in the last 3 months Patients undergoing radiotherapy and chemotherapy Immunosuppressive drugs or corticosteroids during the previous 4 weeks Uncontrolled chronic diseases Malignancy Coagulopathy or the use of anticoagulants History of autoimmune diseases HBV, HCV and HIV infections

Design outcomes

Primary

MeasureTime frame
Side effects. Timepoint: Injection day, and 2 weeks, 1, 2, 4 and 6 months after first injection. Method of measurement: History and clinical examination based on Common Terminology Criteria for Adverse Events criteria.

Secondary

MeasureTime frame
Frontal and vertex hair density. Timepoint: 1, 2, 4, and 6 months after the first injection. Method of measurement: Digital videotrichoscopy.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAmir Bajouri

Tehran University of Medical Sciences

bajouri.md@gmail.com+98 21 2221 2537

Outcome results

None listed

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