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An Interventional Study of Milk Allergy

Primary Purpose

Food Hypersensitivity, Milk Hypersensitivity

Status
Completed
Phase
Early Phase 1
Locations
United States
Study Type
Interventional
Intervention
Baked Milk
Sponsored by
National Institute of Allergy and Infectious Diseases (NIAID)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Food Hypersensitivity focused on measuring Food Allergy, Milk Allergy

Eligibility Criteria

4 Years - 25 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Positive prick skin test to milk and/or detectable serum milk-IgE
  • History of allergic reaction to milk within past 6 months
  • Serum milk-IgE of high predictive value (>15 in children older than 1 year, >5 in children younger than 1 year)
  • Asymptomatic or stabilized atopic disease (asthma, allergic rhinitis, atopic dermatitis) for a minimum of 7 days prior to OFC

Exclusion Criteria:

  • Serum level of cow's milk-specific IgE antibody greater than 35 kIU/L
  • History of anaphylactic reaction to cow's milk within the past 12 months
  • Unstable asthma
  • Allergic eosinophilic gastroenteritis caused by milk
  • Use of short-acting antihistamines more than one time within 3 days of OFC
  • Use of medium-acting antihistamines more than one time within 7 days of OFC
  • Maintenance therapy or use of beta-blockers and ACE inhibitors within 12 to 24 hours of OFC
  • Participation in study baked egg study GCO#03-0609 within 6 months of enrollment
  • Pregnant

Sites / Locations

  • Mount Sinai School of Medicine

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

1

Arm Description

Baked milk and at least 4 oral food challenges as clinically indicated

Outcomes

Primary Outcome Measures

Tolerance to heated milk

Secondary Outcome Measures

Development of tolerance to non-heated milk

Full Information

First Posted
December 19, 2007
Last Updated
July 30, 2012
Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
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1. Study Identification

Unique Protocol Identification Number
NCT00578656
Brief Title
An Interventional Study of Milk Allergy
Official Title
The Impact of the Diet Containing Limited Amounts of Processed Milk Protein on the Natural History of IgE-Mediated Milk Hypersensitivity
Study Type
Interventional

2. Study Status

Record Verification Date
July 2012
Overall Recruitment Status
Completed
Study Start Date
June 2004 (undefined)
Primary Completion Date
February 2011 (Actual)
Study Completion Date
February 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)

4. Oversight

5. Study Description

Brief Summary
Milk is the among the most common food allergens in infants and children. The majority of children outgrow their allergies; however, the exact mechanisms by which food tolerance is achieved are unknown. Strict avoidance of the offending food is currently the only known therapy. However, subjects have been known to lose food hypersensitivity while frequently ingesting small amounts of processed forms of the offending product. The purpose of this study is to investigate whether ingestion of small amounts of processed milk protein will be permitted without compromising the chances of either outgrowing milk hypersensitivity or prolonging the time needed to achieve clinical tolerance.
Detailed Description
In the United States, as many as 6% of children are affected by food allergy. Milk is among the most common food allergens in infants and children. Although strict avoidance of milk is the current standard of care for those with milk hypersensitivity, there is no conclusive evidence that absolute dietary restriction is necessary for achieving clinical tolerance. The purpose of this study is to determine whether ingestion of small amounts of extensively heated milk protein might be permitted without compromising the chances for ultimately losing milk hypersensitivity or prolonging the time needed to achieve clinical tolerance in a selected population of milk-allergic participants. The study will last up to 48 months. Based on the result of the oral food challenge with baked milk the participants will be assigned to either Group 1 (baked milk-tolerant) or Group 2 (baked milk-reactive). Participants in the Group 1 may be further tested with regular, non-heated milk, depending on their diagnostic test results and clinical history. Participants tolerant to non-heated milk will be discharged from the study. Baked milk-tolerant, non-heated milk-reactive participants in Group 1 will receive diet with baked milk at home while Group 2 will act as the control and avoid milk consumption strictly. Qualifying and willing participants will be assigned to Group 1, which will allow consumption of baked milk on a regular basis. Study visits will occur at Months 3, 6, 12, 18, 24, 30, 36, 42, and 48. Participants in Group 1 will be given an OFC using non-heated milk to identify tolerant individuals at Months 12, 24, 36, and 48. Participants in Group 2 will be contacted by telephone every 6 months and asked about the current state of their milk allergy. Participants in this group will be asked to repeat OFC to baked milk at Months 12, 24, 36, and 48. Depending on the outcome of the repeat OFC, they may continue strict avoidance (if they reacted during baked milk OFC) or will be allowed to ingest baked milk in the diet (if they tolerated baked milk OFC). At each visit, medical history, physical exam, 7-day diet record, anthropometric measurements, skin test and blood collection will occur. A pregnancy test will be performed at all visits requiring OFC for females of childbearing potential. A skin prick test will occur at most visits. Participants with atopic dermatitis will be assessed on the SCORAD scale at all visits.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Food Hypersensitivity, Milk Hypersensitivity
Keywords
Food Allergy, Milk Allergy

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Early Phase 1
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
220 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
Baked milk and at least 4 oral food challenges as clinically indicated
Intervention Type
Dietary Supplement
Intervention Name(s)
Baked Milk
Intervention Description
Extensively heated milk
Primary Outcome Measure Information:
Title
Tolerance to heated milk
Time Frame
Throughout study
Secondary Outcome Measure Information:
Title
Development of tolerance to non-heated milk
Time Frame
Throughout study

10. Eligibility

Sex
All
Minimum Age & Unit of Time
4 Years
Maximum Age & Unit of Time
25 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Positive prick skin test to milk and/or detectable serum milk-IgE History of allergic reaction to milk within past 6 months Serum milk-IgE of high predictive value (>15 in children older than 1 year, >5 in children younger than 1 year) Asymptomatic or stabilized atopic disease (asthma, allergic rhinitis, atopic dermatitis) for a minimum of 7 days prior to OFC Exclusion Criteria: Serum level of cow's milk-specific IgE antibody greater than 35 kIU/L History of anaphylactic reaction to cow's milk within the past 12 months Unstable asthma Allergic eosinophilic gastroenteritis caused by milk Use of short-acting antihistamines more than one time within 3 days of OFC Use of medium-acting antihistamines more than one time within 7 days of OFC Maintenance therapy or use of beta-blockers and ACE inhibitors within 12 to 24 hours of OFC Participation in study baked egg study GCO#03-0609 within 6 months of enrollment Pregnant
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hugh A. Sampson, MD
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Scott H. Sicherer, MD
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Anna Nowak-Wegrzyn, MD
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mount Sinai School of Medicine
City
New York
State/Province
New York
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
17935766
Citation
Skripak JM, Matsui EC, Mudd K, Wood RA. The natural history of IgE-mediated cow's milk allergy. J Allergy Clin Immunol. 2007 Nov;120(5):1172-7. doi: 10.1016/j.jaci.2007.08.023. Epub 2007 Nov 1.
Results Reference
background
PubMed Identifier
17919140
Citation
Staden U, Rolinck-Werninghaus C, Brewe F, Wahn U, Niggemann B, Beyer K. Specific oral tolerance induction in food allergy in children: efficacy and clinical patterns of reaction. Allergy. 2007 Nov;62(11):1261-9. doi: 10.1111/j.1398-9995.2007.01501.x.
Results Reference
background
PubMed Identifier
17895338
Citation
Vandenplas Y, Koletzko S, Isolauri E, Hill D, Oranje AP, Brueton M, Staiano A, Dupont C. Guidelines for the diagnosis and management of cow's milk protein allergy in infants. Arch Dis Child. 2007 Oct;92(10):902-8. doi: 10.1136/adc.2006.110999. Erratum In: Arch Dis Child. 2007 Oct;92(10):following 908. Arch Dis Child. 2008 Jan;93(1):93.
Results Reference
background

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An Interventional Study of Milk Allergy

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