Oral Desensitization to Wheat in School Aged Children
Primary Purpose
Wheat Allergy
Status
Completed
Phase
Not Applicable
Locations
Finland
Study Type
Interventional
Intervention
Wheat oral immunotherapy
Sponsored by
About this trial
This is an interventional treatment trial for Wheat Allergy focused on measuring Wheat allergy, Immunotherapy, Desensitization, Food allergy, T cells
Eligibility Criteria
Inclusion Criteria:
- Elevated serum wheat specific IgE
- Immediate reaction in open oral wheat challenge test
- Diet free from wheat, rye, and barley
Exclusion Criteria:
- Uncontrolled asthma
- Other lung disease
- Cardiovascular disease or other significant systemic disease
- Patients having poor compliance
Sites / Locations
- Helsinki University Central Hospital
- Kuopio University Hospital
- University of Oulu
- Tampere University Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Wheat oral immunotherapy
Arm Description
Well-cooked wheat spaghetti is given daily to the patients starting from a minimal dosage (0,0003 g of wheat protein) and increasing the dosing in every 1-2 weeks until a dosage corresponding the size of one meal.
Outcomes
Primary Outcome Measures
Efficacy of oral wheat desensitization
Change in the tolerance to wheat and the amount of daily use of wheat in 3 months after the 5 months oral desensitization therapy.
Secondary Outcome Measures
Efficacy of oral wheat desensitization at 17 months
Change in the tolerance to wheat and the amount of daily use of wheat in 1 year after the 5 months oral desensitization therapy.
Safety of oral wheat desensitization therapy at 8 months
Number of participants with adverse events as a measure of tolerability and safety at 3 months after the 5 months desensitization therapy
Safety of oral wheat desensitization therapy at 17 months
Number of participants with adverse events as a measure of tolerability and safety at 1 year after the 5 months desensitization therapy
Effect of the treatment on the characteristics and function of immune cells
Flow cytometric characterization of the change in the proportions of various T cell subtypes and in the function of these cells in in vitro proliferation and suppression tests between the samples taken before the treatment and 3 and 12 months after the treatment.
Effect of the treatment on the cell specific mRNA expression
qRT-PCR measurement of the change in the expression level of T cell subtype specific mRNA levels between the samples taken before the treatment and 3 and 12 months after the treatment.
Effect of the treatment on the cytokine profile
Flow cytometric measurement of the change in the levels of T cell subtype specific cytokine levels between the samples taken before the treatment and 3 and 12 months after the treatment.
Full Information
NCT ID
NCT01755884
First Posted
December 19, 2012
Last Updated
March 19, 2015
Sponsor
Helsinki University Central Hospital
Collaborators
University of Oulu, Oulu University Hospital, Tampere University Hospital, Kuopio University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT01755884
Brief Title
Oral Desensitization to Wheat in School Aged Children
Official Title
Oral Desensitization to Wheat in Children Over 6 Years of Age With Wheat Allergy
Study Type
Interventional
2. Study Status
Record Verification Date
March 2015
Overall Recruitment Status
Completed
Study Start Date
August 2009 (undefined)
Primary Completion Date
February 2015 (Actual)
Study Completion Date
February 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Helsinki University Central Hospital
Collaborators
University of Oulu, Oulu University Hospital, Tampere University Hospital, Kuopio University Hospital
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The aim of the study is to induce tolerance to wheat in wheat allergic children via oral desensitization therapy. The hypothesis is that oral administration of wheat with increasing dosing will increase the individual threshold for allergic reactivity to wheat protein (i.e. desensitization) and even result in no reactivity (i.e. full tolerance). Along with this, the risk for severe allergic reaction to wheat protein is minimized and the diet of patients can partly or completely be normalized. In addition to clinical measures, the immunological mechanisms of desensitization therapy are studied in detail at cellular and molecular level.
Detailed Description
This is a prospective multicenter study investigating the efficacy, safety and immunological mechanisms of oral wheat desensitization therapy in school-aged (6-16 yrs of age) wheat allergic children. Wheat allergic children with avoidance diet, immediate reaction in a recent (less than 4 months) food challenge test for wheat and elevated serum wheat-specific IgE levels are recruited to the study. Patients having uncontrolled asthma, other lung disease, cardiovascular disease or other significant systemic disease and patients having poor compliance are excluded. Well-cooked wheat spaghetti is given daily to the patients starting from a minimal dosage (0,0003 g of wheat protein) and increasing the dosing in every 1-2 weeks until a dosage corresponding the size of one meal. The initial dosage is given and certain defined dosage step-ups are carried out in the hospital outpatient clinic. The patient and parents are prepared for the emergency treatment of severe allergic reaction and carry adequate medication with them. The daily use of spaghetti continues with the received maintenance dosage for additional 3 months, until the clinical evaluation of the patient. Thereafter, the patients are allowed to use also other wheat products. Peripheral venous blood samples are taken before therapy and at 3 months and 1 year follow-up visits after reaching the maintenance dosage. The characteristics and function of isolated peripheral blood mononuclear cells (PBMC) will be specifically tested using flow cytometric methods. The expression levels of cell-specific mRNAs (messenger ribonucleic acid) and cytokines are measured with qRT-PCR (quantitative reverse transcriptase real-time polymerase chain reaction)and flow cytometry based methods. In addition, specific IgE (immunoglobulin E) levels are measured and serum samples are frozen for further testing. Two separate control groups are also recruited. The first group includes patients with previous food-challenge proven IgE-mediated wheat allergy with spontaneous recovery and the current free use of wheat protein in their diet. The second group includes children (6-16 yrs of age) who come to hospital for a minor surgical operation (e.g. minor trauma, circumcision, patellar luxation etc.). Children with asthma, allergy, atopic eczema, any other chronic disease or recent infection (less than 2 weeks ago) are excluded from this group. Peripheral venous blood samples are taken from all control children. The characteristics and function of isolated PBMCs, the expression levels of cell-specific mRNAs and cytokines and specific IgE levels are measured.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Wheat Allergy
Keywords
Wheat allergy, Immunotherapy, Desensitization, Food allergy, T cells
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
100 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Wheat oral immunotherapy
Arm Type
Experimental
Arm Description
Well-cooked wheat spaghetti is given daily to the patients starting from a minimal dosage (0,0003 g of wheat protein) and increasing the dosing in every 1-2 weeks until a dosage corresponding the size of one meal.
Intervention Type
Dietary Supplement
Intervention Name(s)
Wheat oral immunotherapy
Intervention Description
Cooked spaghetti
Primary Outcome Measure Information:
Title
Efficacy of oral wheat desensitization
Description
Change in the tolerance to wheat and the amount of daily use of wheat in 3 months after the 5 months oral desensitization therapy.
Time Frame
8 months
Secondary Outcome Measure Information:
Title
Efficacy of oral wheat desensitization at 17 months
Description
Change in the tolerance to wheat and the amount of daily use of wheat in 1 year after the 5 months oral desensitization therapy.
Time Frame
17 months
Title
Safety of oral wheat desensitization therapy at 8 months
Description
Number of participants with adverse events as a measure of tolerability and safety at 3 months after the 5 months desensitization therapy
Time Frame
8 months
Title
Safety of oral wheat desensitization therapy at 17 months
Description
Number of participants with adverse events as a measure of tolerability and safety at 1 year after the 5 months desensitization therapy
Time Frame
17 months
Title
Effect of the treatment on the characteristics and function of immune cells
Description
Flow cytometric characterization of the change in the proportions of various T cell subtypes and in the function of these cells in in vitro proliferation and suppression tests between the samples taken before the treatment and 3 and 12 months after the treatment.
Time Frame
17 months
Title
Effect of the treatment on the cell specific mRNA expression
Description
qRT-PCR measurement of the change in the expression level of T cell subtype specific mRNA levels between the samples taken before the treatment and 3 and 12 months after the treatment.
Time Frame
17 months
Title
Effect of the treatment on the cytokine profile
Description
Flow cytometric measurement of the change in the levels of T cell subtype specific cytokine levels between the samples taken before the treatment and 3 and 12 months after the treatment.
Time Frame
17 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Elevated serum wheat specific IgE
Immediate reaction in open oral wheat challenge test
Diet free from wheat, rye, and barley
Exclusion Criteria:
Uncontrolled asthma
Other lung disease
Cardiovascular disease or other significant systemic disease
Patients having poor compliance
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mika J Mäkelä, MD, PhD
Organizational Affiliation
Helsinki University Central Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Helsinki University Central Hospital
City
Helsinki
ZIP/Postal Code
00029
Country
Finland
Facility Name
Kuopio University Hospital
City
Kuopio
ZIP/Postal Code
70211
Country
Finland
Facility Name
University of Oulu
City
Oulu
ZIP/Postal Code
90014
Country
Finland
Facility Name
Tampere University Hospital
City
Tampere
ZIP/Postal Code
33521
Country
Finland
12. IPD Sharing Statement
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Oral Desensitization to Wheat in School Aged Children
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