Full Text View
Tabular View
No Study Results Posted
Related Studies
An Interventional Study of Milk Allergy
This study is ongoing, but not recruiting participants.
Study NCT00578656   Information provided by National Institute of Allergy and Infectious Diseases (NIAID)
First Received: December 19, 2007   Last Updated: February 24, 2009   History of Changes

December 19, 2007
February 24, 2009
June 2004
November 2011   (final data collection date for primary outcome measure)
Tolerance to heated milk [ Time Frame: Throughout study ] [ Designated as safety issue: Yes ]
Same as current
Complete list of historical versions of study NCT00578656 on ClinicalTrials.gov Archive Site
Development of tolerance to non-heated milk [ Time Frame: Throughout study ] [ Designated as safety issue: Yes ]
Same as current
 
An Interventional Study of Milk Allergy
The Impact of the Diet Containing Limited Amounts of Processed Milk Protein on the Natural History of IgE-Mediated Milk Hypersensitivity

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.

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. The participants will be assigned to either Group 1 or Group 2. Group 1 will receive treatment with baked milk while Group 2 will act as the control and avoid milk consumption. This study will include dose escalation followed by oral food challenge (OFC).

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 baked milk to identify desensitized 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 perform OFC at Months 12, 24, 36, and 48.

At each visit, medical history, physical exam, 7-day diet record, anthropometric measurements, and blood collection will occur. A pregnancy test will be performed at all visits 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.

Phase 0
Interventional
Diagnostic, Non-Randomized, Open Label, Parallel Assignment
  • Food Hypersensitivity
  • Milk Hypersensitivity
  • Dietary Supplement: Baked Milk
  • Dietary Supplement: Baked milk placebo
  • Experimental: Baked milk and at least 4 oral food challenges as clinically indicated
  • Placebo Comparator: Placebo for baked milk and at least 4 oral food challenges as clinically indicated

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Active, not recruiting
220
November 2011
November 2011   (final data collection date for primary outcome measure)

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 cosinophilic 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 ot 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
Both
4 Years to 25 Years
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00578656
Associate Director, Clinical Research Program, DAIT/NIAID
DAIT P01 AI 144236, GCO#01-1209
National Institute of Allergy and Infectious Diseases (NIAID)
 
Principal Investigator: Hugh A. Sampson, MD
Principal Investigator: Scott H. Sicherer, MD
Principal Investigator: Anna Nowak-Wegrzyn, MD
National Institute of Allergy and Infectious Diseases (NIAID)
August 2007

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP