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临床试验/NCT00292812
NCT00292812已完成不适用

The Clinical Effects of an Infant Formula Supplemented With Various Concentrations of Nucleotides

Soroka University Medical Center2 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2006年3月最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
150
试验地点
2
主要终点
Growth percentiles, Behaviour and infantile colic, Bowel habits.

研究概览

简要总结

The study hypothesis is that different concentrations of nucleotides' supplementation of an infant formula might affect differently growth and/or other clinical parameters in neonates.

详细描述

Three groups of 50 newborn infants each, will be fed for 30 days an infant formula supplemented with either 4.9 mg/100 kcal or 10.6 mg/100 kcal of nucleotides or with no supplementation. Newborns will be monitored prospectively for the following outcome parameters:

  • Growth percentiles.
  • Behaviour and infantile colic.
  • Bowel habits.
  • Side effects.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Double

入排标准

年龄范围
1 Day 至 30 Days(Child)
性别
All
接受健康志愿者

入选标准

  • Healthy newborns aged 0-30 days.

排除标准

  • Prematurity
  • Chronic illness
  • Failure to thrive
  • Milk allergy

结局指标

主要结局

Growth percentiles, Behaviour and infantile colic, Bowel habits.

次要结局

  • Side effects.

研究者

申办方类型
Other

研究点 (2)

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