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Efficacy and safety of cell therapy for androgenetic alopecia

Single-Center Randomized Controlled Clinical Study on Autologous Hair Follicle Cell Transplantation for Treating Male Androgenetic Alopecia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600124601
Enrollment
Unknown
Registered
2026-05-14
Start date
2026-05-20
Completion date
Unknown
Last updated
2026-05-18

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

Conditions

Androgenetic alopecia (AGA)

Interventions

Intervention Group:autologous hair follicle unit cell transplantation
Control Group:Finasteride 1mg qd

Sponsors

Dermatology Hospital of Shandong First Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 49 Years

Inclusion criteria

Inclusion criteria: 1.Aged 18-49years, male; 2.Clinical diagnosis of AGA at the time of screening according to the Chinese Guidelines for the Diagnosis and Treatment of Androgenetic Alopecia 2014; 3.The Norwood-Hamilton grade for male hair loss was III-v~V; 4.No alopecia treatment, systemic or topical medications with hair regrowth effects, and physical therapy in the 6 month prior to inclusion; 5.Voluntary participation in this clinical study.

Exclusion criteria

Exclusion criteria: 1.Combined with other types of hair loss such as patchy baldness, scarring alopecia, etc. 2.hose who are allergic to any of the components of the applied drugs; 3.Patients who are afraid of needles or faint of needles; 4.Patients with blood system diseases such as coagulation disorders, or patients with Scalp Psoriasis, severe seborrheic dermatitis, severe Folliculitis, serious Infections, and other diseases that make it difficult to stop bleeding after injury; 5.Moderate to severe abnormalities of liver and kidney function, or suffering from serious organic or systemic diseases.

Design outcomes

Primary

MeasureTime frame
Improvement rate from baseline in target area non-vellus hair count (TAHC);

Secondary

MeasureTime frame
Change in hair follicle density per unit area in the target region compared to baseline;Change in Hamilton–Norwood grade relative to baseline;Adverse Event (AE);Change from baseline in mean non-vellus hair shaft diameter in the target area;Change in target area hair density per unit area relative to baseline;

Countries

China

Contacts

Public ContactGuoyan Liu

Dermatology Hospital of Shandong First Medical University

wfliuguoyan@126.com+86 5318729827

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 22, 2026