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Investigating the new method of exosome therapy comparing to PRP in the treatment of hair loss

Assessing the effect of exosome therapy in the treatment and control of hair loss and comparing it with PRP

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20181005041243N5
Enrollment
100
Registered
2024-11-07
Start date
2025-03-21
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

hair loss. Androgenic alopecia

Interventions

Intervention 1: First intervention group: Exosome solution is injected on the head every month for 4 months. This solution will be made by Razi hospital laboratory. Intervention 2: Second intervention

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Aged 18-60 Clinical diagnosis of androgenic alopecia with a dermatologist Have not received any drug for alopecia in the past 12 months

Exclusion criteria

Exclusion criteria: Pregnancy or breastfeeding during the intervention history of internal diseases, including endocrine diseases causing alopecia alteration in diet and lifestyle during the study polycystic ovary syndrome The disease caused by another reason than androgenic alopecia Consuming any systemic or topical drugs which caused hair loss or hair regrowth Have a history of hair transplantation History of skin diseases which cause hair loss like cutaneous cancers, infection, psoriasis photosensitivity

Design outcomes

Primary

MeasureTime frame
Hair regrrowth score. Timepoint: At the beginning of the study (before the start of the intervention) and 6 months after the start of trial. Method of measurement: Hair regrowth score based on the observations of two dermatologists assessing the before and after photographs.

Secondary

MeasureTime frame
Patients' satisfaction with androgenic alopecia recovery. Timepoint: At the beginning of the study (before the start of the intervention) and 6 months after the start of trial. Method of measurement: Visual Analogue Scale.;Hair regrowth score based on Fotofinder device. Timepoint: At the beginning of the study (before the start of the intervention) and 6 months after the start of trial. Method of measurement: Hair density (hairs/cm2) and Hair diameter (hairs/cm2).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZeinab Aryanian

Tehran University of Medical Sciences

z_aryanian@yahoo.com+98 21 5563 0553

Outcome results

None listed

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