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Effects of an Ultrasound Focusing Device for Noncontact Force Radiation on Hair.

Effects of an Ultrasound Focusing Device for Noncontact Force Radiation on Hair. - Effects of an Ultrasound Focusing Device for Noncontact Force Radiation on Hair.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000038797
Enrollment
12
Registered
2019-12-05
Start date
2019-12-13
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

N/A(healthy adults)

Interventions

Radiating an ultrasound on measurement point (20 minutes / time
16 times). Nonradiating an ultrasound on measurement point (20 minutes / time
16 times).

Sponsors

TES Holdings Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: [1]Healthy Japanese females aged 20-29 years. [2]Individuals who are healthy and have no chronic physical disease including skin disease. [3]Individuals whose working space is indoors. [4]Individuals whose written informed consent has been obtained. [5]Individuals who can have an examination on a designated check day. [6]Individuals judged appropriate for the study by the principal.

Exclusion criteria

Exclusion criteria: [1]Individuals using medical products. [2]Individuals with thinning hair or male pattern baldness. [3] Individuals with skin disease, such as atopic dermatitis on scalp. [4]Individuals who used a drug to treat Androgenetic Alopecia in the past 3 months. [5]Individuals who used a drug to treat a disease in the past 1 month. [6]Individuals who have a history of serious hepatopathy, kidney damage, heart disease, hematological and blood disease. [7]Individuals who contract or have a history of serious gastrointestinal disease. [8]Individuals whose BMI is over 30.0. [9]Individuals who have a habit to use a similar treatment with the test method or other hair growth promotion method. [10]Individuals who have an addiction to alcohol or a mental illness. [11]Individuals with possible changes of life style during the test period. [12]Individuals who participated in other clinical studies in the past 3 months. [13]Individuals judged inappropriate for the study by the principal.

Design outcomes

Primary

MeasureTime frame
[1]Analysis of the number of hairs, the hair density, and the anagen:telogen ratio with TrichoScan (Week 0 and just after hair cutting, Week 0 and 3 days after hair cutting, Week 16 and just after hair cutting, Week 16 and 3 days after hair cutting).

Secondary

MeasureTime frame
*Secondary outcomes [1]Gene expression test on a hair cycle (Week 0 and just after hair cutting, Week 16 and just after hair cutting). [2]Questionnaire of physical feeling (Week 0 and just after hair cutting, Week 16 and just after hair cutting). *Safety [1]Visual examination of head by a medical doctor (Screening, Week 0 and just after hair cutting, Week 16 and just after hair cutting). [2]Doctor's questions (Screening, Week 0 and just after hair cutting, Week 16 and just after hair cutting). [2]Subject's diary (From the first day of ingestion of a test material to the last day of the test).

Countries

Japan

Contacts

Public ContactRyoma Shimizu

TES Holdings Co., Ltd. Administrative Department of Clinical Trials

r.shimizu@tes-h.co.jp+81-3-6801-8480

Outcome results

None listed

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