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Evaluate changes in atopic symptoms due to natural mineral water intake

Not Applicable
Conditions
Healthy adult
Registration Number
JPRN-UMIN000038511
Lead Sponsor
Japan Clinical Trial Association
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
26
Inclusion Criteria

Not provided

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

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Blood test,Urinalysis, VAS, visual evaluation by doctor, subjective evaluation
Secondary Outcome Measures
NameTimeMethod
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