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临床试验/NCT05418491
NCT05418491已完成不适用

A Post-intervention Follow-up of the Allergy Reduction Trial, to Investigate the Prolonged Risk Reducing Effect of a Partially Hydrolysed Infant Formula During the First Six Months of Life on Allergic Manifestations Up to the Age of 5 Years

FrieslandCampina3 个研究点 分布在 3 个国家目标入组 455 人开始时间: 2022年7月21日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
455
试验地点
3
主要终点
Incidence of allergic Manifestations

研究概览

简要总结

The present study is a 5-year follow-up of the Allergy Reduction Trial (A.R.T.) birth cohort study of 551 infants at high-risk for allergy. The A.R.T. 5-year follow-up study, aims to investigate the prolonged effect of each feeding regimen [formula-fed (exclusively or partially) with the partially hydrolyzed formula (pHF) or the standard formula (SF), or exclusively breastfed] within the first 6 months of life on the development of any allergic manifestations up to the age of 5 years. Allergic manifestations within this time period will include the presence of any of the following: atopic dermatitis, food allergies, respiratory allergies, urticaria, drug allergy and insect venom allergy. In addition, differences on growth (weight, height, BMI) will be examined.

详细描述

The present study is a 5-year follow-up of the Allergy Reduction Trial (A.R.T.) birth cohort study of 551 infants at high-risk for allergy. The A.R.T. 5-year follow-up study, aims to investigate the prolonged effect of each feeding regimen [formula-fed (exclusively or partially) with the partially hydrolyzed formula (pHF) or the standard formula (SF), or exclusively breastfed] within the first 6 months of life on the development of any allergic manifestations up to the age of 5 years. Allergic manifestations within this time period will include the presence of any of the following: atopic dermatitis, food allergies, respiratory allergies, urticaria, drug allergy and insect venom allergy. In addition, differences on growth (weight, height, BMI) will be examined.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Cross Sectional

入排标准

年龄范围
5 Years 至 63 Months(Child)
性别
All
接受健康志愿者

入选标准

  • Children who were part of the Intention-to-Treat population of the A.R.T. study
  • Children of the A.R.T. study ITT population within the age range of 5 years up to 5 years and 3 months
  • Children of the A.R.T. study ITT population in whom at least one parent and/or legal guardian signed the written consent form

排除标准

  • Children who did not participate in the A.R.T. study or who were not assigned to any of the 3 study arms
  • Children of the A.R.T. study who are younger than 5 years of age or older than 5 years and 3 months of age
  • Children of the A.R.T. study in whom parents and/or guardians do not agree to provide a written consent form

结局指标

主要结局

Incidence of allergic Manifestations

时间窗: At 5 years of age

Incidence of allergic manifestations (AM) based on parental reporting using Childhood Allergy questionnaire comparing partially hydrolyzed protein formula, standard formula and exclusive breastfeeding.

次要结局

未报告次要终点

研究者

发起方
FrieslandCampina
申办方类型
Industry
责任方
Sponsor

研究点 (3)

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