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临床试验/NCT03661736
NCT03661736已完成不适用

Growth of Infants With Cow's Milk Allergy Fed an Amino Acid-based Formula Containing Two Human Milk Oligosaccharides: Comparison With World Health Organization (WHO) Growth Standards in an Observational, Single-arm Study

Société des Produits Nestlé (SPN)1 个研究点 分布在 1 个国家目标入组 33 人开始时间: 2018年4月12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
33
试验地点
1
主要终点
The weight-for-age z-score (WAZ) compared with the WHO 2006 Child Growth Standard

研究概览

简要总结

The main aim of this study is to provide longitudinal growth data in infants with moderate-to-severe cow's milk allergy fed an amino acid-based formula with two added human milk oligosaccharides.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
1 Month 至 8 Months(Child)
性别
All
接受健康志愿者

入选标准

  • Full term infant (37 weeks ≤ gestation ≤ 42 weeks)
  • 2500g ≤ birth weight ≤ 4500g
  • Having obtained written informed consent form the infant's parents or legally authorized representatives (LAR).
  • Infant aged between 1 and 8 months.
  • Exclusively formula-fed at time of enrolment; or CMPA infant receiving partial breastfeeding and infant's mother having independently elected before enrolment to exclusively formula feed.
  • Infants with physician-diagnosed CMPA as per standard clinical practice:

排除标准

  • Previous treatment with AAF > 72 hours
  • Known underlying medical condition that would impair growth (as per physician's assessment, e.g. unstable congenital heart disease, cystic fibrosis, metabolic disorder, chronic liver disease etc.)
  • Demonstrated chronic malabsorption which is not due to CMPA.
  • Other significant pre-natal and/or serious post-natal disease other than CMPA before enrolment (per investigator's medical decision).
  • Infants whose parents or caregivers who cannot give informed consent or who cannot be expected to comply with study procedures.
  • Treatment with systemic corticosteroids (oral or intravenous) for >72 hours within 4 weeks before enrolment (topical corticosteroids allowed)
  • Infants taking probiotic preparations for > 72 hour within 4 weeks before enrolment
  • Currently participating or having participated in another clinical trial since birth.

结局指标

主要结局

The weight-for-age z-score (WAZ) compared with the WHO 2006 Child Growth Standard

时间窗: Comparison of baseline WAZ vs WAZ at 4 months

Weight gain will be measured in kg and converted to WAZ scores

次要结局

  • Length-for-age Z-scores (LAZ) compared with the WHO 2006 Child Growth Standard(1, 2, 3, 4 months from baseline and at 12 months of age)

研究者

发起方
Société des Produits Nestlé (SPN)
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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