Ireland
--:--IST
Starting soon Not applicable

A Split-Scalp Study Evaluating the Efficacy and Safety of Fractional Laser Therapy With and Without Exosomes in the Treatment of Androgenetic Alopecia

NCT07248410 · tracked via the Priya Life Science Taiwan tracker
Phase
Not applicable
Started
2025-11-24
Last updated
2025-11-25

Condition(s) studied

Androgenetic Alopecia

Investigational drug(s) / intervention(s)

fraction laser

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

Sex
MALE
Min age
18 Years
Max age
50 Years
Healthy volunteers
No
Inclusion Criteria: 1. Male pattern baldness diagnosed according to the Norwood-Hamilton classification III-V 2. Males aged 18 to 50 years 3. Willing to provide written informed consent and possessing the ability to read, write, speak, and understand 4. Able to follow the study's treatment guidelines Exclusion Criteria: 1. Those who have taken oral Finasteride, Dutasteride, or Minoxidil within 6 months prior to the start of the trial. 2. Those who have used any topical or systemic medications that may affect hair growth within 6 months prior to the start of the trial. 3. Those who have received phototherapy, laser therapy, exosome therapy, or hair regrowth injections (such as minimally invasive procedures) within 6 months prior to the start of the trial. 4. Those with a history of hair transplant surgery. 5. Those suffering from other systemic or scalp diseases that may affect hair growth (e.g., iron deficiency anemia, immune disorders, thyroid diseases, and syphilis). 6. Those with a history of severe inflammation, keloids, malignant tumors, or poor wound healing at the treatment site. 7. Those with other diseases that make them unsuitable for fractional laser treatment. 8. Those with a history of malignant tumors or currently undergoing treatment. 9. Participants must not undergo any cosmetic procedures that may affect scalp condition or hair growth throughout the entire trial period, including hair dyeing, perming, bleaching, scalp exfoliation, deep scalp cleansing, or any other actions that may irritate or damage the scalp.

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)

FacilityCityRegionStatus
Chang Gung Memorial Hospital Taoyuan branch Taoyuan Taoyuan
Official registry record

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