Food Hypersensitivity Clinical Trial
Official title:
Evaluation of Hypoallergenicity of an Amino Acid-Based Infant Formula
Verified date | June 2013 |
Source | Nestlé |
Contact | n/a |
Is FDA regulated | No |
Health authority | United States: Institutional Review Board |
Study type | Interventional |
The primary objective of this clinical trial is to determine whether a new amino acid-based formula is hypoallergenic as defined by the American Academy of Pediatrics (2000), demonstrating that the test formula does not provoke allergenic activity in 90% of infants or children with confirmed cow's milk allergy (CMA) with 95% confidence as compared to a commercially available hypoallergenic formula.
Status | Completed |
Enrollment | 37 |
Est. completion date | April 2013 |
Est. primary completion date | April 2013 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 2 Months to 12 Years |
Eligibility |
Inclusion Criteria: - Born at term (>36 weeks gestation) - 2 months to =12 years of age at enrollment - Documented CMA within 6 months prior to enrollment - Otherwise healthy - Asthma, atopic dermatitis and/or rhinitis must be well-controlled, if applicable - Expected daily intake of at least 8 oz (240ml) of the study formula during the open challenge phase - Having obtained his/her legal representative's informed consent Exclusion: - Children consuming mother's milk at the time of inclusion and during the trial - Any chromosomal or major congenital anomalies - Any major gastrointestinal disease or abnormalities other than CMA - Chronic medical diseases (ie seizure disorders, chronic lung disease, heart problems (heart murmurs okay) - Immunodeficiency - Anti-histamine use in 7 days prior to the first food challenge (eyedrops are permitted) - Oral steroid use within 14 days prior to enrollment (intranasal and topical corticosteroid use are permitted) - Unstable asthma - Severe uncontrolled eczema - Severe anaphylactic reaction to milk within the last 2 years - Severe anaphylactic reaction to breastmilk within the last 2 years - Subject who in the Investigator's assessment cannot be expected to adhere to the study protocol - Currently participating in another clinical trial. |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention
Country | Name | City | State |
---|---|---|---|
United States | Georgia Pollens Clinical Research Centers Inc. | Albany | Georgia |
United States | TTS Research | Boerne | Texas |
United States | Deaconess Clinic, Inc. | Evansville | Indiana |
United States | Allergy & Asthma Physicians | Hinsdale | Illinois |
United States | Pediatric Care Medical Group, Inc. | Huntington Beach | California |
United States | Mount Sinai Medical Center | New York | New York |
United States | ENT & Allergy Associates | Newburgh | New York |
United States | Clinical Research Partners | Richmond | Virginia |
United States | Allergy & Asthma Medical Group and Research Center, A P.C. | San Diego | California |
Lead Sponsor | Collaborator |
---|---|
Nestlé |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | occurrence of allergic reactions | occurrence of allergic reactions to double-blind placebo controlled food challenge (DBPCFC) | 14 days | Yes |
Secondary | Digestive Tolerance | gastrointestinal tolerance and formula intake recorded during the open challenge phase. | one week | No |
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