Effect and safety of supplementation of Lactobacilli powder to the patients with atopic dermatitis accompanied by food allergy
Not Applicable
- Conditions
- atopic dermatitis
- Registration Number
- JPRN-UMIN000006209
- Lead Sponsor
- PO Allergy Support Network
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Not provided
Exclusion Criteria
1. Suspected NOT to be able to take the powder food daily. 2. Clinical history of severe anaphylaxis caused by the small amount of milk product. 3. Any severe complications such as diabetes, gastrointestinal, renal, or heart diseases. 4. Clinical history of hypersensitivity to steroid ointment, skin moisturizer or the test food. 5. Undergoing or planning any other intervention study. 6. Any other inappropriate conditions judged by the participant doctors.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Decrease in SCORAD index after 24 week
- Secondary Outcome Measures
Name Time Method QOL, Dose of topical corticosteroid, intestinal flora, eosinophils, IgE, LDH, AST, ALT, TARC after 24 weeks