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临床试验/NCT02132663
NCT02132663已完成不适用

The Effects on Growth and Tolerance of a Routine Infant Formula Fed to Term Infants

Mead Johnson Nutrition44 个研究点 分布在 1 个国家目标入组 315 人开始时间: 2014年5月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
315
试验地点
44
主要终点
Body weight measured at each study visit

研究概览

简要总结

This clinical trial will evaluate an investigational infant formula with an alternate source of DHA to determine if it provides normal growth and if it is well tolerated by term infants as compared to a marketed routine infant formula.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • Singleton, 10-14 days of age at randomization
  • Term infant with birth weight of a minimum of 2500 grams
  • Solely formula fed
  • Signed Informed Consent and Protected Health Information

排除标准

  • History of underlying metabolic or chronic disease or immunocompromised
  • Feeding difficulties or formula intolerance

研究组 & 干预措施

Infant formula containing an alternate source of DHA

Experimental

干预措施: An investigational infant formula containing an alternate source of DHA (Other)

Marketed routine infant formula

Active Comparator

干预措施: Control: Marketed routine infant formula (Other)

结局指标

主要结局

Body weight measured at each study visit

时间窗: 3.5 Months

次要结局

  • Body length measured at each study visit(3.5 months)
  • Recall of stool consistency measured at each study visit(3.5 months)
  • Recall of gastrointestinal tolerance measured at each study visit(3.5 months)
  • Blood Collection(Once at 120 days of age)
  • Medically-confirmed adverse events collected throughout the study period(3.5 months)
  • Head circumference measured at each study visit(3.5 months)
  • Recall of infant formula intake at each study visit(3.5 months)

研究者

发起方
Mead Johnson Nutrition
申办方类型
Industry
责任方
Sponsor

研究点 (44)

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