Cow's Milk Allergy Clinical Trial
Official title:
Evaluation of Hypoallergenicity of a New Extensively Hydrolyzed Formula
Verified date | July 2017 |
Source | Nestlé |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Infants/children with cow's milk allergy will take part in 2 double-blinded placebo-controlled food challenges (DBPCFC) of 2 extensively hydrolyzed formulas in random order. If both food challenges are passed, subjects will be asked to consume the Test formula in an at-home open challenge for 7 days.
Status | Completed |
Enrollment | 83 |
Est. completion date | June 2017 |
Est. primary completion date | June 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 2 Months to 4 Years |
Eligibility |
Inclusion Criteria: - Born at term (>36 weeks gestation) - 2 months to <4 years of age at enrollment - Documented CMA within 6 months prior to enrollment - Otherwise healthy - Having obtained his/her legal representative's informed consent Exclusion Criteria: - Children consuming mother's milk at the time of inclusion and during the trial - Any chromosomal or major congenital anomalies - Chronic medical diseases (ie seizure disorders, chronic lung disease, heart problems (heart murmurs okay)) - Immunodeficiency - Receiving free amino acid formula - Subject who in the Investigator's assessment cannot be expected to adhere to the study protocol - Currently participating in another clinical trial. |
Country | Name | City | State |
---|---|---|---|
United States | Allergy and Sinus Relief Center/Great Lakes Medical research | Chardon | Ohio |
United States | Atria Clinical Research | Little Rock | Arkansas |
United States | Allergy and Asthma Associates of Southern California | Mission Viejo | California |
United States | Mt. Sinai | New York | New York |
United States | ENT & Allergy Associates | Newburgh | New York |
United States | All Children's Hospital | Saint Petersburg | Florida |
United States | AeroAllergy | Savannah | Georgia |
United States | Allergy Asthma Research Institute | Waco | Texas |
Lead Sponsor | Collaborator |
---|---|
Nestlé |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | allergic reaction | number of children who react during a DBPCFC to either formula | 2 hours post-DBPCFC | |
Secondary | stool characteristics | stool descriptors as collected on daily diaries | 1 week | |
Secondary | formula intake | amount of formula ingested as collected on daily diaries | 1 week | |
Secondary | adverse events | any adverse event reported by caregivers | 1 week |
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