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A Clinical Study on the Efficacy and Safety of Microneedle Delivery of a Recombinant Collagen Solution for the Treatment of Androgenetic Alopecia

A Clinical Study on the Efficacy and Safety of Microneedle Delivery of a Recombinant Collagen Solution for the Treatment of Androgenetic Alopecia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600127547
Enrollment
Unknown
Registered
2026-07-02
Start date
2026-07-15
Completion date
Unknown
Last updated
2026-07-13

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

Conditions

Androgenetic alopecia

Interventions

Treatment group:Microneedle Delivery of a Recombinant Collagen Complex Solution

Sponsors

Yan'an University Xianyang Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Clinically diagnosed with androgenetic alopecia and meeting the diagnostic criteria outlined in the *2023 Clinical Practice Guidelines: Diagnosis and Treatment of Androgenetic Alopecia*; 2. Have not used any oral or topical hair loss medications in the past six months; 3. Aged 18–60 years,gender is not restricted; 4. Hair loss is not caused by skin diseases such as leprosy or syphilis, or by trauma or medication; 5. Not currently pregnant or breastfeeding; 6. Willing to sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1. A history of androgenetic alopecia lasting more than 10 years; 2. Having undergone other hair loss treatments within the past 3 months; 3. A history of malignant tumors, platelet dysfunction, anemia, or bleeding disorders; 4. HIV-positive, hepatitis B-positive, or hepatitis C-positive; 5. Impaired immune function; 6. Active skin disease or skin infection in the treatment area; 7. Currently taking nonsteroidal anti-inflammatory drugs (NSAIDs); 8. Tendency to develop keloids.

Design outcomes

Primary

MeasureTime frame
Hair condition;Effectiveness evaluation;

Secondary

MeasureTime frame
Satisfaction Score;Quality of Life Rating;Scalp symptoms;Safety;

Countries

China

Contacts

Public ContactXiaoyan Chen

Yan'an University Xianyang Hospital

631146340@qq.com+86 29 33785591

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026