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Clinical observation on the anti hair loss efficacy of electric laser hair generator instruments

Clinical observation on the anti hair loss efficacy of electric laser hair generator instruments

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300077470
Enrollment
Unknown
Registered
2023-11-09
Start date
2023-11-13
Completion date
Unknown
Last updated
2023-11-13

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

Conditions

Hair Loss

Interventions

Test group:Use of electric laser hair generator instruments and anti detachment products
Control group:Use of electric laser hair generator instruments

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) 18-60 years old, healthy male or female; (2) Hair length between 5-40 cm; (3) Those who suffer from excessive hair loss and mild thinning of hair, and have a hair loss count of more than 10 hairs according to the 60 comb method, and still have more than 10 hairs after 2 weeks of hair washing period; (4) Those who have not undergone special hair treatments such as dyeing, perming, or styling within the past month; (5) Those who can understand the experimental process, voluntarily participate in the experiment, and sign a written informed consent form.

Exclusion criteria

Exclusion criteria: (1) Pregnant or lactating women, or those who have recently planned for pregnancy; (2) Patients with severe androgenic alopecia, alopecia areata, inflammatory scar alopecia, or other scalp/hair diseases; (3) Individuals with mental or psychological disorders; Or those with long-term sleep or emotional control disorders; (4) Those who have used cosmetics or other products with anti hair loss effects or hair growth effects within the past 3 months; (5) Those who have taken or locally used any medication that affects hair growth within the past 6 months; (6) Those who have received hair transplant treatment; (7) Hair curlers; (8) Highly sensitive individuals with high physical fitness; (9) Those who have participated in other clinical trials within the past 2 months; (10) Clinical evaluation suggests that it is not suitable for participants in the trial.

Design outcomes

Primary

MeasureTime frame
Hair loss count;Take a photo of the entire head of hair;clinical evaluation;Subject self-assessment;MoleMaxHD+Trichoscan of local photography;Safety assessment;

Countries

China

Contacts

Public ContactWang Xi

West China Hospital, Sichuan University

xierwang@126.com+86 28 8542 2075

Outcome results

None listed

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