Efficacy and safety of slow and rush oral immunotherapy for patients with food allergy
Not Applicable
Recruiting
- Conditions
- Food allergy
- Registration Number
- JPRN-UMIN000019699
- Lead Sponsor
- Kansai Medical University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Not provided
Exclusion Criteria
1) severe bronchial asthma 2) severe atopic dermatitis 3) acute severe illenes 4) Decision of ineligibility by a physician
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Evaluation of the symptom provocation threshold change at the time of entry and 12 months after the start of oral immunotherapy and frequencies of allergic symptoms during the 12 months.
- Secondary Outcome Measures
Name Time Method 1. Analysis of immunologic parameters in blood samples and measurements of prick test at entry, food challenge and 1 year late the entry. 2. Analysis of adverse effects during this clinical study.