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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03667118
Other study ID # STU00205862
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 18, 2017
Est. completion date October 9, 2017

Study information

Verified date March 2019
Source Northwestern University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of the study is to test a food supplement to:

- Show that the food supplement is well tolerated and safe to feed to infants;

- Find out how often parents/caregivers feed their infants the food supplement;

- Find out how parents/caregivers usually add the food supplement to infants' regular solid or liquid food; and

- Learn what aspects of the food supplement are more or less attractive to infants and to parents/caregivers.


Description:

The study involves parents/caregivers of infants, ≥ 5 months but < 11 months of age. Parents who enrolled their infants complete a 1-month blinded placebo run-in period, followed by randomization to placebo or the food supplement.

During the intervention period, infants randomized to the food supplement are fed a once daily, individual packet of the food supplement mixed into liquid (e.g., breast milk, infant formula) or solid (e.g., applesauce, pureed carrots) foods being fed to the infant. The food supplement is a blend of 16 common allergenic proteins ([oat, milk, egg, sesame, wheat] [almond cashew, hazelnut, peanut, pecan, pistachios, soy, walnut] [cod, shrimp, salmon]) combined with 400 IU of Vitamin D3. Parents complete a daily diary about any reactions or symptoms within 2 hours of ingesting the food supplement. Infants randomized to the placebo are also fed a once daily individual packet of the placebo mixed into liquid or solid foods being fed to the infant. Parents also complete a daily diary about any reactions or symptoms within 2 hours of ingesting the placebo.


Recruitment information / eligibility

Status Completed
Enrollment 705
Est. completion date October 9, 2017
Est. primary completion date October 9, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 5 Months to 11 Months
Eligibility Inclusion Criteria:

- healthy infants, = 5 months but < 11 months of age whose parent/caregiver can provide, in English, consent, understand instructions and complete a daily diet diary for their child, answer questions about how much and in what food they mix the Food supplement, and report any reaction or adverse event. Pregnant women will not be excluded if they have a child who is eligible for the study.

Exclusion Criteria:

- - Any parent/caregiver who cannot provide consent.

- Any parent/caregiver who cannot understand or write English.

- A parent/caregiver who is in prison.

- Any infant who

- Has a previous or current diagnosis of food allergy, made by a board-certified allergy and immunology specialist;

- Was born before 37 weeks of pregnancy (premature birth);

- Has severe eczema, as determined by two parent/caregiver questions:

1. During the past 6-11months, have you been told by a doctor or other health professional that your infant has eczema or any kind of skin allergy? (National Health Interview Survey, 2012) If yes, go to Question 2.

2. Would you describe (his/her) eczema or skin allergy as mild, moderate, or severe? (National Survey of Children's Health, 2007) If described as severe, infant is excluded.

- Has a current serious, chronic condition, as measured by:

1. Does you infant have a health condition that has lasted for more than three (3) months? If yes, go to Question 2.

2. Has your infant been hospitalized more than 2 times since birth for this condition? If yes to Question 1 and 2, infant is excluded.

- If a parent/caregiver has multiple birth infants (e.g., twins), only one eligible infant will be selected.

- Any person who works for Before Brands or who has a family member working for Before Brands.

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Food Supplement
A powder blend of 16 common allergenic proteins ([oat, milk, egg, sesame, wheat] [almond cashew, hazelnut, peanut, pecan, pistachios, soy, walnut] [cod, shrimp, salmon]) combined with 400 IU of Vitamin D3

Locations

Country Name City State
United States Jane L Holl Chicago Illinois

Sponsors (1)

Lead Sponsor Collaborator
Northwestern University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Allergic-type reaction difference between the proportion of infants with allergic-type reaction within 2 hours of ingestion in the food supplement versus placebo arm 1month
Secondary Symptom difference between the proportion of infants with a symptom within 2 hours of ingestion of the food supplement versus placebo arm 1 month
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