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Study of the Effects on Hair Growth in Women with Thinning Hair on Continuous Use of TMD1 Hair Growth Products

Study of the Effects on Hair Growth in Women with Thinning Hair on Continuous Use of TMD1 Hair Growth Products - Study of the Effects on Hair Growth in Women with Thinning Hair on Continuous Use of TMD1 Hair Growth Products

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000052684
Enrollment
51
Registered
2023-11-05
Start date
2023-11-06
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Hair thinning

Interventions

Placebo TMD1 hair growth product applied to the scalp twice daily for 24 weeks Apply a middle concentration of TMD1 hair growth product to the scalp twice daily for 24 weeks Apply a high concentration

Sponsors

TMC Medical Corporation,Tokyo Memorial Clinic
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Asian women between the ages of 45 and 65 2. Subjects with thinning hair equivalent to Ludwig Scale I-2 to II-2 3. Subjects who have been informed of the purpose and content of the study prior to the study, have the capacity to make decisions, and have given their written consent.

Exclusion criteria

Exclusion criteria: 1. Those who have undergone hair transplantation 2. Persons who have dyed, bleached or permanent hair within 3 months of the screening test. 3. Persons who may show allergic symptoms to test substance components. 4. Persons who may show skin allergy symptoms or skin hypersensitivity. 5. Persons with a history of serious heart disease, renal disease, liver disease, cancer, or thyroid dysfunction in the past. 6. Persons who have not used health foods, cosmetics, quasi-drugs, or medicines that may affect the test results for more than 6 months. 7. Women who are pregnant or possibly pregnant and women who are breast-feeding 8. Other persons whom the principal investigator deems inappropriate to be included in the study.

Design outcomes

Primary

MeasureTime frame
Percentage change in number of hairs after 24 weeks of use

Countries

Japan

Contacts

Public ContactHiromu Katsuta

Re-Life.inc Clinical Development Division

hkatsuta@relife-inc.com03-5985-0077

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026