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Polynucleotides for hair regrowth in androgenetic alopecia

Polynucleotides for hair regrowth in androgenetic alopecia

Status
Unknown
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20240525004
Enrollment
30
Registered
2024-05-25
Start date
2024-04-17
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Androgenetic alopecia Androgenetic alopecia, Polynucleotides, Hair loss, Hair thinning, Hair regrowth, VEGF, angiogenesis.

Interventions

Polynucleotides injectable
Experimental Drug
Rejuran classic

Sponsors

Rejuran
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1.AGA Hamilton-Norwood Stages III to V (including Type III vertex) were enrolled. Subjects must maintain the normal hair length, color and style during the study. 2.Female pattern hair loss Ludwig type I-II

Exclusion criteria

Exclusion criteria: 1. Patients who are not interested or deny about this study. 2. Patient who is undertaking treatment for disease before this study periods: 2.1 Treatment with topical medication within 6 months 2.2 Treatment with systemic medication (Finasteride within 12 months,Minoxidil within 12 months, Dutasteride within 18 months) 2.3 Using shampoo for hair growth stimulation (non- medicated) treatment or taking hair supplements within 3 months. 2.4Treatment with oral supplement within 12 months 2.5 Using shampoo for hair growth stimulation (non- medicated) treatment or taking hair supplements within 3 months 2.6 Any other treatment for hair growth within 1 month. 3. Patient with alopecia other than androgenetic alopecia 4. Patient with other systemic disease like malnutrition, autoimmune disease, symptomatically immunocompromised disease like HIV, syphilis and cancer. 5. Patient with lack of cooperation as well as psychological disorder. 6. Patient with history of hair transplantation or restoration surgery. 7. Patient who is unreliable or poor compliance

Design outcomes

Primary

MeasureTime frame
hair density, hair diameter every 1 month, for 4 months dermoscope,photograph

Secondary

MeasureTime frame
satisfaction every 1 month,for 4 months 7 point improvement scale

Countries

Thailand

Contacts

Public ContactJitlada Meephansan

Thammasat university

pr.cicm.tu@gmail.com025644440

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026