Time-limited Specific Oral Tolerance Induction in Children With Severe Egg Allergy (EGGSOTI)
Primary Purpose
- Egg Hypersensitivity
Status
Completed
Phase
Phase 1
Locations
Italy
Study Type
Interventional
Intervention
Specific oral tolerance induction
Sponsored by
About this trial
This is an interventional treatment trial for - Egg Hypersensitivity focused on measuring Egg allergy,specific oral tolerance induction
Eligibility Criteria
Inclusion Criteria:
- at least 1 anaphylactic reaction (grade 3, 4 and 5 according to Sampson's grading after accidental exposure to trace amounts of egg or egg-derivative products, requiring emergency treatment, at least 1 year before enrollment
- demonstration of egg white specific IgE by the skin prick test (SPT), end-point SPT, raw egg white prick-by-prick (PP) and egg white-specific IgE determination
- positive double-blind placebo-controlled food challenge (DBPCFC) at a dose of less than 0.9 ml of raw emulsion egg
Exclusion Criteria:
- age below 5 years
- poorly controlled asthma
- parents with a history of unreliable management of complications and treatment.
Sites / Locations
- Unit of Pediatrics, Fatebenefratelli Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Specific oral tolerance induction
control
Arm Description
Specific oral tolerance induction consisted in the administration of increasing amounts of food antigen
controls were kept on an egg-free diet for 6 months
Outcomes
Primary Outcome Measures
Number of Children That Achieved Total (40 ml) or Partial (Less Than 40 ml But at Least 10 ml) Tolerance to Raw Egg
To evaluate the efficacy of a 6-month Specific Oral Tolerance Induction (SOTI) protocol in inducing tolerance (maximal dose of raw egg emulsion tolerated after 6 months) in children with severe IgE-mediated egg allergy and a history of at least 1 anaphylactic reaction after accidental exposure to egg.
Secondary Outcome Measures
Changes in the Median Weal Diameter, Using Egg White SPTs, End-point SPT and PP
Before and after SOTI, we evaluated the change in the median weal diameter in millimeters, using egg white SPTs, end-point SPT and PP.
Full Information
NCT ID
NCT01379651
First Posted
June 20, 2011
Last Updated
September 19, 2011
Sponsor
Ospedale Buon Consiglio Fatebenefratelli
1. Study Identification
Unique Protocol Identification Number
NCT01379651
Brief Title
Time-limited Specific Oral Tolerance Induction in Children With Severe Egg Allergy
Acronym
EGGSOTI
Official Title
Specific Oral Tolerance Induction in Children With Severe Egg Allergy: A Randomized Controlled Trial Using a 6 Months Protocol
Study Type
Interventional
2. Study Status
Record Verification Date
September 2011
Overall Recruitment Status
Completed
Study Start Date
January 2008 (undefined)
Primary Completion Date
June 2010 (Actual)
Study Completion Date
June 2010 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ospedale Buon Consiglio Fatebenefratelli
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
To evaluate the efficacy of a 6-month specific oral tolerance induction (SOTI) protocol in inducing tolerance (maximal dose of raw egg emulsion tolerated) in children with severe IgE-mediated egg allergy and a history of at least 1 anaphylactic reaction after accidental exposure to egg.
Detailed Description
Oral immunotherapy consisted in the administration of increasing amounts of raw emulsion egg. The children started with 1 drop of undiluted raw egg emulsion (0.05 ml) flavored with vanilla and cacao, hidden by the parents in the child's breakfast (cow's milk, soymilk, fruit juice or other). The dose was doubled at intervals of about one month in the day hospital. The increases in dose were customized for each subject based on the frequency and severity of side effects, or when an inter-current illness or asthma worsening intervened during the SOTI.
The investigators limited the SOTI protocol to six months for all patients, irrespective of the dose reached, in order to favor the adherence of families to the study.
When objective symptoms seemed more important (grade 2, 3 and 4 reaction), medical treatment was given. Subjects were discontinued from the study in case of severe adverse reactions (grade 5 reaction). Parents were advised they could telephone investigators 24 hours a day
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
- Egg Hypersensitivity
Keywords
Egg allergy,specific oral tolerance induction
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
20 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Specific oral tolerance induction
Arm Type
Experimental
Arm Description
Specific oral tolerance induction consisted in the administration of increasing amounts of food antigen
Arm Title
control
Arm Type
No Intervention
Arm Description
controls were kept on an egg-free diet for 6 months
Intervention Type
Other
Intervention Name(s)
Specific oral tolerance induction
Other Intervention Name(s)
SOTI
Intervention Description
Specific oral tolerance induction consisted in the administration of increasing amounts of raw emulsion egg
Primary Outcome Measure Information:
Title
Number of Children That Achieved Total (40 ml) or Partial (Less Than 40 ml But at Least 10 ml) Tolerance to Raw Egg
Description
To evaluate the efficacy of a 6-month Specific Oral Tolerance Induction (SOTI) protocol in inducing tolerance (maximal dose of raw egg emulsion tolerated after 6 months) in children with severe IgE-mediated egg allergy and a history of at least 1 anaphylactic reaction after accidental exposure to egg.
Time Frame
baseline and 6 months
Secondary Outcome Measure Information:
Title
Changes in the Median Weal Diameter, Using Egg White SPTs, End-point SPT and PP
Description
Before and after SOTI, we evaluated the change in the median weal diameter in millimeters, using egg white SPTs, end-point SPT and PP.
Time Frame
Baseline and 6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
5 Years
Maximum Age & Unit of Time
11 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
at least 1 anaphylactic reaction (grade 3, 4 and 5 according to Sampson's grading after accidental exposure to trace amounts of egg or egg-derivative products, requiring emergency treatment, at least 1 year before enrollment
demonstration of egg white specific IgE by the skin prick test (SPT), end-point SPT, raw egg white prick-by-prick (PP) and egg white-specific IgE determination
positive double-blind placebo-controlled food challenge (DBPCFC) at a dose of less than 0.9 ml of raw emulsion egg
Exclusion Criteria:
age below 5 years
poorly controlled asthma
parents with a history of unreliable management of complications and treatment.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Iride Dello Iacono, pediatrician
Organizational Affiliation
Unit of Pediatrics, Fatebenefratelli Hospital, Benevento, Italy
Official's Role
Study Director
Facility Information:
Facility Name
Unit of Pediatrics, Fatebenefratelli Hospital
City
Benevento
ZIP/Postal Code
82100
Country
Italy
12. IPD Sharing Statement
Citations:
PubMed Identifier
20355360
Citation
Calvani M, Giorgio V, Miceli Sopo S. Specific oral tolerance induction for food. A systematic review. Eur Ann Allergy Clin Immunol. 2010 Feb;42(1):11-9.
Results Reference
background
PubMed Identifier
12777599
Citation
Sampson HA. Anaphylaxis and emergency treatment. Pediatrics. 2003 Jun;111(6 Pt 3):1601-8.
Results Reference
background
PubMed Identifier
16455349
Citation
Sicherer SH, Sampson HA. 9. Food allergy. J Allergy Clin Immunol. 2006 Feb;117(2 Suppl Mini-Primer):S470-5. doi: 10.1016/j.jaci.2005.05.048.
Results Reference
background
PubMed Identifier
19076011
Citation
Barbi E, Berti I, Longo G. Food allergy: from the of loss of tolerance induced by exclusion diets to specific oral tolerance induction. Recent Pat Inflamm Allergy Drug Discov. 2008 Nov;2(3):212-4. doi: 10.2174/187221308786241875.
Results Reference
background
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Time-limited Specific Oral Tolerance Induction in Children With Severe Egg Allergy
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