Status:

RECRUITING

6-Month Trial of Chinese Herbal Treatments for Hair Loss and Gray Hair

Lead Sponsor:

Vita Green Pharmaceutical (H.K.) Ltd.

Conditions:

Alopecia

Canities

Eligibility:

All Genders

18-60 years

Phase:

NA

Brief Summary

This will be a 6-month randomized, double-blind, placebo-controlled trial. A total of 152 participants with hair loss, including some with gray hair, will be enrolled and randomly assigned to four gro...

Eligibility Criteria

Inclusion

  • Participants must sign the informed consent form prior to enrollment and fully understand the study's purpose, procedures, and potential adverse events.
  • Adults aged 18 to 60 years, both male and female; each group must include no less than 50% female participants.
  • Hair length must be greater than 5 cm.
  • Women must meet the Savin scale classification between grades 1-3 to II.
  • Men must meet the Norwood-Hamilton classification between stages II and VI.
  • At least 10 participants in each group must have gray hair, with a minimum of 5 gray hairs within a 1 cm × 4 cm area of the scalp.
  • Participants must not have undergone any special hair treatments-such as dyeing, perming, or styling-within the past two months.

Exclusion

  • Pregnant or breastfeeding women, or individuals planning to conceive in the near future.
  • Individuals with medical conditions causing hair loss, such as refractory alopecia areata, inflammatory scarring alopecia, or psoriatic alopecia; or those diagnosed with other scalp or hair disorders.
  • Individuals with diagnosed psychiatric or psychological disorders, or those with long-term sleep disturbances or emotional regulation issues.
  • Use of anti-hair loss cosmetics or other hair growth-promoting products within the past 3 months.
  • Use of any systemic or topical medications known to affect hair growth within the past 6 months.
  • History of hair transplantation.
  • Curly hair.
  • Individuals with highly sensitive constitutions.
  • Individuals diagnosed with severe anemia or abnormal liver/kidney function during physical examination.
  • Participation in any other clinical trials involving the test area within the past 2 months.
  • Any other conditions deemed unsuitable for participation by the clinical investigators.

Key Trial Info

Start Date :

July 30 2025

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

October 30 2026

Estimated Enrollment :

152 Patients enrolled

Trial Details

Trial ID

NCT06998680

Start Date

July 30 2025

End Date

October 30 2026

Last Update

September 19 2025

Active Locations (1)

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Page 1 of 1 (1 locations)

1

The First People's Hospital of Xiangtan City

Xiangtan, Hunan, China, 411100