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临床试验/NCT03667118
NCT03667118已完成不适用

Daily Ingestion of a Multi-Allergen Food Supplement by Infants: Clinical Symptoms, Reactions, and Acceptability - A Randomized Trial

Northwestern University2 个研究点 分布在 1 个国家目标入组 705 人开始时间: 2017年6月18日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
705
试验地点
2
主要终点
Allergic-type reaction

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Single (Participant)

盲法说明

Parents received packets of the powder to be fed from their infant directly from the manufacturer.

入排标准

年龄范围
5 Months 至 11 Months(Child)
性别
All
接受健康志愿者

入选标准

  • 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.

排除标准

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

研究组 & 干预措施

Food Supplement

Experimental

Infants who received the active food supplement powder

干预措施: Food Supplement (Dietary Supplement)

Placebo

Placebo Comparator

Infants who received the placebo powder

干预措施: Food Supplement (Dietary Supplement)

结局指标

主要结局

Allergic-type reaction

时间窗: 1month

difference between the proportion of infants with allergic-type reaction within 2 hours of ingestion in the food supplement versus placebo arm

次要结局

  • Symptom(1 month)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Jane Holl

Director, Center for Healthcare Studies

Northwestern University

研究点 (2)

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