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An open label single group study to investigate the effect of granular ceramic treated water with ELCE (R) showerhead on dry skin.

An open label single group study to investigate the effect of granular ceramic treated water with ELCE (R) showerhead on dry skin. - Clinical trial to investigate the effect of granular ceramic treated water with ELCE (R) showerhead on dry skin.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000046366
Enrollment
14
Registered
2021-12-20
Start date
2021-12-21
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 adult

Interventions

Use the ELCE (R) showerhead for 8 weeks.

Sponsors

University of Miyazaki
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Subjects who are judged as healthy by self-reported health questionnaire. 2. Subjects who have symptom of dry skin. 3. Subjects who agree to participate in this study with a written informed consent after receiving sufficient explanation relating to this study.

Exclusion criteria

Exclusion criteria: 1. Subjects who answered in the self-reported health questionnaire that they currently have a skin disease that requires treatment. 2. Subjects who answered in the self-reported health questionnaire that they have had or are currently suffering from respiratory, gastrointestinal, hepatic/gallbladder/pancreatic, hematologic, renal, endocrine, cardiovascular and/or mental disease that requires hospital treatment. 3. Subjects who had a serious injury or surgical history within 12 weeks prior to this study. 4. Heavy smokers (more than 21 cigarettes per day), alcohol addicts (more than 80g per day alcohol), subjects who are alcohol or drug dependence, subjects who are suspected of alcohol or drug dependence. 5. Subjects who are undergoing special facial care (e.g. facial appliances, aesthetic treatments, peels, laser treatments, etc.) which would affect this study. 6. Subjects who are pregnant or lactating, or subjects who expect to be pregnant during this study. 7. Subjects who have cognitive disorder or who have possibility of the disorder. 8. Subjects who participated and took the study drug in other clinical trials within four weeks prior to this study. 9. Subjects who are judges as unsuitable for this study by the principal investigator or subinvestigators.

Design outcomes

Primary

MeasureTime frame
VAS evaluation of "skin hydration" for subjective skin condition assessment after 8 weeks of using the ELCE (R) showerhead.

Secondary

MeasureTime frame
1. VAS evaluation of subjective skin conditions other than "skin hydration". 2. Satisfaction with the use of the ELCE (R) showerhead. 3. Percutaneous moisture evaporation. 4. Stratum corneum moisture content. 5. Adverse events.

Countries

Japan

Contacts

Public ContactYasuji Arimura

University of Miyazaki Health-Care Research Department, University of Miyazaki

yasuji_arimura@med.miyazaki-u.ac.jp0985-85-9577

Outcome results

None listed

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