The effect verification examination by continuous use of bath additives

The effect verification examination by continuous use of bath additives - The continuous use examination of bath additives

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000026027

Enrollment

Registered

2017-03-01

Start date

2017-03-01

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

Healthy adults

Interventions

Bathe with bath additives A for 10 minutes once a day for 4 weeks Bathe with bath additives B for 10 minutes once a day for 4 weeks Bathe with bath additives C for 10 minutes once a day for 4 weeks Ba

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: Healthy females

Exclusion criteria

Exclusion criteria: (1) Subjects who has a cutaneous symptom which affects the final examination in the body (2) Subjects who are using the drugs which may influence an examination (3) Subjects (except for dental care) under a therapy or going to hospital regularly due to sick. (4) Subjects who has pollinosis (5) Subjects past menopause (6) Subjects under pregnancy or who may have been conceived, and breast-feeding (7) Subjects who has participated in other clinical trials (8) Subjects judged that a test implementation person in charge is unsuitable

Design outcomes

Primary

Measure	Time frame
Evaluation of fatigue, sleep, body composition, an autonomic nerve function, a vascular function, and blood composition before use of bath additives and after continuous use for 2 and 4 weeks	—

Countries

Japan

Contacts

Public ContactKazunori Takashima

INFORWARD inc. EBISU Skin research center

takashima@inforward.co.jp03-5793-8712

Outcome results

None listed

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