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Comparison of efficacy of exosomes vs platelet rich plasma therapy in treatment of androgenetic alopecia

Comparison of efficacy of exosomes vs platelet rich plasma therapy in treatment of androgenetic alopecia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12625000548437
Enrollment
50
Registered
2025-05-30
Start date
2025-01-01
Completion date
2025-06-30
Last updated
2025-09-08

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

Conditions

None listed

Brief summary

OBJECTIVE This study aims to compare the efficacy of exosomes versus PRP in the treatment of Androgenetic alopecia by using photographic assessment, hair pull test and patient self-assessment questionnaire over a period of 6 months. HYPOTHESIS Exosomes are expected to be significantly more effective then PRP in treatment of AGA.

Interventions

This study aims to compare the efficacy of exosomes versus PRP in the treatment of Androgenetic alopecia by using photographic assessment, hair pull test and patient self-assessment questionnaire over a period of 6 months. The enrolled patients will be randomly divided into two groups using the lottery method, Group A and B, each with 40 participants. GROUP A: Group A will receive treatment with exosomes intradermally at 0,1 and 3 months. Exosomes used are GFC CELL, consist of Leucoexo 97% havi

This study aims to compare the efficacy of exosomes versus PRP in the treatment of Androgenetic alopecia by using photographic assessment, hair pull test and patient self-assessment questionnaire over a period of 6 months. The enrolled patients will be randomly divided into two groups using the lottery method, Group A and B, each with 40 participants. GROUP A: Group A will receive treatment with exosomes intradermally at 0,1 and 3 months. Exosomes used are GFC CELL, consist of Leucoexo 97% having GFC CELL EXO SCALP 9700 powder and EXO SCALP Pep9 solution. The scalp will be cleaned with spirit and nerve block will be given by using the local injection, lignocaine, by insulin syringe at supratrochlear, supraorbital, and occipital region. Exosomes will then be injected at a strength of 2 to 10 billion particles/5ml, at a dose of 0.1 ml/cm2 of scalp. Patients will be observed for 1-hour post procedure for any adverse effects and will be instructed not to wash or massage their hair and avoid heavy activities for 48 hours after the injection. Exosomes will be administered by Dermatologist in the dermatology clinic, Combined Military Hospital, Quetta. Participants will be assessed at 0,1, 3, and 6 months. Serial photographs will be taken at each assessment. The efficacy of both groups will be evaluated using the hair pull test, global photography, patient and physician satisfaction questionnaire.

Sponsors

Dr Maira Wajahat - Combined Military Hospital Quetta
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Primary purpose
Treatment
Masking
Blinded (masking used) (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

Inclusion criteria Clinical diagnosis of AGA Age range of 18-60 years Platelets count more than 150, 000 /µl to 450,000/ µl Patients with Hamilton-Norwood Grade 2-5 or Ludwig scale Grade 1-3 Patients who haven’t received topical or systemic treatments for AGA within 3 months prior to the study Patient who gave consent for the study

Exclusion criteria

Exclusion criteria Patients with other causes of hair loss fungal infection such as fungal infection, inflammatory or scarring alopecia, hyper-androgenism, telogen effluvium or other hormonal disorders Patients with history of severe systemic disease (renal, cardiovascular hepatic and lungs) or active cancers Pregnant or breastfeeding patients Patients having known hypersensitivity to exosomes Patients that are immunodeficient or are undergoing immunosuppressive therapy Patients on anticoagulation or having bleeding disorders such as thrombocytopenia and anemia

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026