Efficacy of oral tolerance induction by Kakkonto in food allergy
Not Applicable
Completed
- Conditions
- food allergy
- Registration Number
- JPRN-UMIN000030175
- Lead Sponsor
- Toyama University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Not provided
Exclusion Criteria
1.Complication or past history of heart, liver and kidney diseases. 2.Uncontrolled asthma, atopic dermatitis, allergic rhinitis 3.Children who were judged as inappropriate by the study director
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Induced reaction during 24 weeks of treatment 2. Change of dose threshold in oral food challenge after 24 weeks of treatment 3. adverse reaction of kakkonto
- Secondary Outcome Measures
Name Time Method 4. Specific IgE/IgG4 antibody, cytokines, lymphocytes subsets 5. Prick test 6. Compliance of kakkonto