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A Split-Scalp Study Evaluating the Efficacy and Safety of Fractional Laser Therapy With and Without Exosomes in the Treatment of Androgenetic Alopecia
Sponsor: Chang Gung Memorial Hospital
Summary
This trial aims to evaluate the efficacy, safety, and tolerability of fractional laser combined with topical exosome for hair regrowth in patients with androgenetic alopecia. This study is expected to recruit 30 participants. The experimental group will receive fractional laser treatment combined with human umbilical cord mesenchymal stem cell exosome solution; the control group will receive fractional laser treatment combined with a placebo. Participants will receive three fractional laser treatments and will be followed up for 6 months. At each follow-up visit, hair density, diameter, vellus hair to terminal hair ratio, and adverse reactions will be assessed using trichotomy; a global photographic assessment will be performed using standardized imaging equipment.
Key Details
Gender
MALE
Age Range
18 Years - 50 Years
Study Type
INTERVENTIONAL
Enrollment
30
Start Date
2025-11-24
Completion Date
2027-10-31
Last Updated
2025-11-25
Healthy Volunteers
No
Conditions
Interventions
fraction laser
We will performed the fraction laser on the scalp of participants with energy of 30-40mJ every month for 3 times.
Locations (1)
Chang Gung Memorial Hospital Taoyuan branch
Taoyuan District, Taoyuan, Taiwan