A Split-Scalp Study Evaluating the Efficacy and Safety of Fractional Laser Therapy With and Without Exosomes in the Treatment of Androgenetic Alopecia
Condition(s) studied
Investigational drug(s) / intervention(s)
fraction laser: We will performed the fraction laser on the scalp of participants with energy of 30-40mJ every month for 3 times.
Study 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.
Eligibility
Primary outcome measure(s)
- Change in hair density (d84) — Baseline to Day 84
Evaluation of the change in hair density of fractional laser combined with exosomes in improving hair growth
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Chang Gung Memorial Hospital Taoyuan branch | Taoyuan | Taoyuan |
More Chang Gung Memorial Hospital trials in Taiwan
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07248410 on ClinicalTrials.gov ↗ ← All trials in Taiwan