The Utility of Food-Specific IgE Measured With the IMMULITE 2000 Assay to Predict Symptomatic Food Allergy
IMMULITE 2000
2 other identifiers
observational
102
1 country
1
Brief Summary
Food allergy is on the rise within the pediatric population. Having food allergy can cause medical, nutritional and psychological issues in those who suffer with it. Although making the appropriate diagnosis of food allergy is very important, properly diagnosing food allergy has been a challenge. Skin prick testing and food-specific IgE testing of the blood can give positive results that are false. Currently, Oral Food Challenges are the best way to diagnose a food allergy. Unfortunately, Oral Food Challenges are time consuming and may not be readily available to suspected food allergy sufferers. This study is designed to examine the effectiveness of an allergy-detecting blood test called IMMULITE 2000 manufactured by the study sponsor, Siemens.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Sep 2013
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2013
CompletedFirst Submitted
Initial submission to the registry
September 23, 2013
CompletedFirst Posted
Study publicly available on registry
September 25, 2013
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 29, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
March 29, 2017
CompletedOctober 19, 2020
October 1, 2020
3.6 years
September 23, 2013
October 15, 2020
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Relationship between food specific IgEs
To determine the relationship between food-specific IgE to whole proteins of milk, egg, and peanut using the IMMULITE 2000 assay and OFC outcomes.
approximately 2 weeks
Secondary Outcomes (1)
Logisitic regression analyses on data
approximately 2 weeks
Study Arms (3)
Peanut allergic
Subjects allergic to peanuts by oral food challenge
Milk allergic
Subjects allergic to milk by oral food challenge
Egg allergic
Subjects allergic to egg by oral food challenge
Interventions
Confirmation of allergy to egg, milk and/or peanut through an oral food challenge or documentation of a positive oral food challenge.
Eligibility Criteria
Study population will be primarily obtained from the pediatric clinic at National Jewish Health from those suspected of egg, milk and/or peanut food allergy.
You may qualify if:
- Age 3 to 21 years of either sex and any race
- Physician-diagnosed food allergy or convincing clinical history of food allergy to milk, egg, and/or peanut AND a Skin prick test positive to milk, egg, and/or peanut (diameter of wheal \> 3 mm or greater than negative control) orOR a detectable serum food-specific IgE level (ImmunoCAP and/or IMMULITE \> 0.35 kUA/L) to milk, egg, and/or peanut
- If no history of clinical reactivity to milk, egg, or peanut, then a positive skin prick test to milk, egg, and/or peanut (diameter of wheal \> 3 mm or greater than negative control) OR a detectable serum food-specific IgE level within the previous 4 months to milk, egg, and/or peanut
- Written informed consent from parent/guardian and assent (when age appropriate).
- Willingness to submit specimen for laboratory serum IgE testing
You may not qualify if:
- Inability to discontinue antihistamines for skin prick testing and OFCs
- Current allergy to placebo ingredient (oat flour) OR reaction to any dose of placebo at the qualifying OFC
- FEV1 value \<80% predicted OR any clinical features of moderate or severe persistent asthma, as defined by the 2007 NHLBI guidelines table for classifying asthma baseline severity (Step 3 or above), at the time of entry into the study
- Use of , and \>high medium daily doses of inhaled corticosteroids, as defined by the 2007 NHLBI guidelines inhaled corticosteroid dosing table (500500 μg/day fluticasone or equivalents for an adult) or a long acting beta-agonist (LABA) to control asthma.
- Asthma requiring either:
- \> 1 hospitalization in the past year for asthma or \> 1 ER visit in the past 6 months for asthma
- History of intubation due to allergies or asthma
- Use of steroid medications (IV, IM or oral) for asthma in the following manners:
- history of daily oral steroid dosing for \>1 month during the past year or
- burst or steroid course/burst in the past 3 months or
- \>2 burst oral steroid courses/bursts in the past year
- History of intubation due to allergies or asthma
- Life-threatening allergic reaction (e.gi.e., respiratory compromise, hypoxia, hypotension, use of epinephrine) to study food(s) (e.g., milk, egg, and/or peanut) within last 1 year
- Diagnosis of active eosinophilic gastrointestinal disease in the past year
- Severe or poorly controlled atopic dermatitis, as assessed by a three-item severity (TIS) score of 6 or greater (see Appendix I)
- +5 more criteria
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
National Jewish Health
Denver, Colorado, 80206, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Erwin Gelfand, MD
National Jewish Health
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 23, 2013
First Posted
September 25, 2013
Study Start
September 1, 2013
Primary Completion
March 29, 2017
Study Completion
March 29, 2017
Last Updated
October 19, 2020
Record last verified: 2020-10