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Evaluate changes in atopic symptoms due to natural mineral water intake

Evaluate changes in atopic symptoms due to natural mineral water intake : a double-blind, randomized placebo-controlled and parallel study - Evaluate changes in atopic symptoms due to natural mineral water intake

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000038511
Enrollment
24
Registered
2019-11-12
Start date
2019-11-12
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

Ingest test article (for 12 weeks) Ingest placebo (for 12 weeks)

Sponsors

Japan Clinical Trial Association
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Subjects who suffer from mild atopic symptoms 2. Subjects with skin dryness and sensitive skin

Exclusion criteria

Exclusion criteria: 1. Subjects who are pregnant or breastfeeding 2.Subjects who are severe or moderate in the classification of symptoms of atopic dermatitis 3. Subjects participating in other human trial 4. Subjects who are scheduled to receive treatment that affects the inflammatory site during the study period

Design outcomes

Primary

MeasureTime frame
Blood test,Urinalysis, VAS, visual evaluation by doctor, subjective evaluation—

Countries

Japan

Contacts

Public ContactTakeshi Kaneko

Japan Clinical Trial Association N.A.

info@yakujihou.org0364574666

Outcome results

None listed

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