跳至主要内容
临床试验/NCT05508750
NCT05508750已完成不适用

A Randomized, Controlled Trial Evaluating Growth and Safety in Infants Fed a New Infant Formula

Jovie USA, LLC1 个研究点 分布在 1 个国家目标入组 420 人开始时间: 2022年9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
420
试验地点
1
主要终点
Weight gain from baseline to 16 weeks feeding

研究概览

简要总结

The aim of this study is to assess age-appropriate growth of healthy infants fed a new infant formula. In this randomized, controlled trial, healthy, term, formula-fed infants will be randomized to one of two infant formulas: a standard, commercially-available infant formula for term infants or the new infant formula for term infants for 16 weeks. A reference group of human milk-fed infants will also be enrolled. This study is designed in accordance with Good Clinical Practice guidelines and the requirements of the Code of Federal Regulations, 21CFR106.96. This study allows caregivers to participate completely from the comfort of their own home.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Triple (Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
0 Days 至 14 Days(Child)
性别
All
接受健康志愿者

入选标准

  • Normal term infant (37-42 weeks gestation at birth)
  • Infant <15 (+3) days of age at first study feeding, Birth constitutes day 0
  • Infant birth weight of ≥2500 g (5.5 lbs.)
  • Healthy Infant
  • Caregiver who has previously decided to exclusively feed infant formula or exclusively breastfeed and is willing to continue with current feeding method throughout the study (breastfeeding or formula feeding)
  • Caregiver willing to conform to protocol requirements (e.g. measuring, feeding, completion of food intake and tolerance diaries, and reporting of AEs)
  • Caregiver willing and able to sign informed consent

排除标准

  • Infant born in multiple birth (i.e., twins, triplets, etc.)
  • Infant born with medical complications (e.g., neurological, cerebral palsy, etc.)
  • Infant with family history (parents or siblings) of confirmed Milk or Soy allergies
  • Infant with failure to thrive, fever, any GI tract abnormalities (e.g., short gut, gastroesophageal reflux, etc.), any congenital illness or malformation that may affect infant feeding or normal growth
  • Caregiver intent to feed non-study formula or solid food during the study

结局指标

主要结局

Weight gain from baseline to 16 weeks feeding

时间窗: 16 weeks

Weight gain g/day

次要结局

  • Length gain from baseline to 16 weeks feeding(16 weeks)
  • Head Circumference gain from baseline to 16 weeks feeding(16 weeks)
  • Volume of formula consumed during 3-consecutive day intervals(16 weeks)

研究者

发起方
Jovie USA, LLC
申办方类型
Industry
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验