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A randomized controlled clinical trial on the efficacy and safety of a hydrogen-enriched herbal hair growth solution in the treatment of hair loss

A randomized controlled clinical trial on the efficacy and safety of a hydrogen-enriched herbal hair growth solution in the treatment of hair loss - H2-Herbal Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600128489
Enrollment
Unknown
Registered
2026-07-21
Start date
2025-04-27
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Alopecia

Interventions

Drinking purified water+hair growth solution group:Use the herbal scalp cleansing liquid once every two days: take 10ml, apply it to the scalp, gently massage for 5–10 minutes, then rinse with clean w
Drinking hydrogen water+hair growth solution group:The intervention method is consistent with Group 1, except that the drinking water is replaced with hydrogen-rich water. Canned hydrogen water of the
Drinking purified water+regular shower+hair growth solution group:A standardized shower requirement is added on the basis of Group 1: take a shower once every two days, preferably at 20:00 p.m. ± 60 m
Drinking hydrogen water+hydrogen water shower+hair growth solution group:A hydrogen-rich water shower is added on the basis of Group 2: take a shower once every two days at the same time as Group 3, c

Sponsors

Shanghai Changhai Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Healthy males and females aged between 18 and 60. 2. The hair length is between 5-40cm. 3. Having mild to moderate hair loss or thinning, at least one of the following criteria must be met: a. BASP classification: M1-M3 or V1-V2, female F1-F2; b. Sinclair rating: 2-3 levels; c. 60 combing methods: The number of hair loss is greater than 10, and it still exceeds 10 after a 2-week washing period. 4. I have not undergone any hair styling treatments such as dyeing or perming in the past month. 5. Willing to comply with the research protocol and sign a written informed consent form.

Exclusion criteria

Exclusion criteria: 1. Pregnant, lactating women, or women with plans to conceive. 2. Individuals with severe scalp diseases such as androgenetic alopecia and alopecia areata. 3. Individuals with mental disorders or long-term sleep problems. 4. Those who have received hair transplant treatment or recently participated in other clinical trials. 5. Individuals deemed unsuitable for the trial based on clinical evaluation.

Design outcomes

Primary

MeasureTime frame
Hair loss count;hair density;Hair shaft diameter;

Secondary

MeasureTime frame
scalp health;Treatment compliance and satisfaction;

Countries

China

Contacts

Public ContactShang Yan

The First Affiliated Hospital of Naval Medical University (Shanghai Changhai Hospital)

wangqian_0508@163.com+86 159 0174 9250

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026