跳至主要内容
临床试验/NCT02096302
NCT02096302已完成不适用

Evaluar el Efecto de Una fórmula Infantil Enriquecida Con el probiótico CECT7210 Sobre la Incidencia de Infecciones Gastrointestinales

Laboratorios Ordesa3 个研究点 分布在 1 个国家目标入组 194 人开始时间: 2011年1月1日最近更新:
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
194
试验地点
3
主要终点
Changes in diarrhea incidence

研究概览

简要总结

The purpose of this study is to determine whether an infant formula supplemented with a new probiotic CECT7210, is effective in reducing the incidence of infections, specially the gastrointestinal ones.

详细描述

This a multicenter, controlled, randomized, prospective, parallel, double-blinded study to evaluate the effect of an infant formula containing a new probiotic, Bifidobacterium longum biovar infantis CECT7210, on the incidence of diarrhea in healthy infants born at term. Infants will be randomized to take an standard infant formula or the infant formula with the probiotic CECT7210 during 12 weeks.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
— 至 90 Days(Child)
性别
All
接受健康志愿者

入选标准

  • Full-term healthy newborns (>= 37 weeks)
  • Birth weight between >=2.500g and <=4.500g)
  • Normal growth curve (between 3-97 percentiles)
  • 0-60 days of age on enrolment
  • Maximum 30 days of breastfeeding
  • Exclusively infant formula on enrolment
  • Breastfeeding or infant formula with pre/probiotics feeding stopped 15 days before enrolment
  • Parents or caregivers agree to exclude any source of prebiotics or probiotics during the study
  • Parents or caregivers agree to follow-on the study 12 weeks
  • Informed consent signed ( Parent/Legal representative)

排除标准

  • Congenital illness or malformation that may affect infant feeding and /or normal growth
  • Significant pre-natal or post-natal diseases
  • Infant's family history of atopy
  • Any pathology related to the immune or gastrointestinal system.
  • Suspected or known allergy to cow's milk protein
  • Infants receiving pre or probiotics within less than 15 days prior to enrolment
  • Infant's family who in the investigator's assessment cannot be expected to comply with the protocol

研究组 & 干预措施

Experimental Formula

Experimental

Infant formula with a novel probiotic CECT7210

干预措施: Infant Formula with a novel probiotic CECT7210 (Dietary Supplement)

Standard Formula

Active Comparator

Standard infant formula without probiotics

干预措施: Standard formula (Dietary Supplement)

结局指标

主要结局

Changes in diarrhea incidence

时间窗: At 4th, 8th, 12th weeks

Differences between diarrhea incidence amongst groups from baseline to 12th weeks.

次要结局

  • Changes in infections incidence(At 4th, 8th, 12th weeks.)
  • Tolerability of the product(At 4th, 8th and 12th weeks)
  • Growth(At 4th, 8th and 12th weeks)
  • Changes in microbiota(At 4th, 8th, 12th weeks)
  • Changes in Immunoglobulin A secretor (IgAs)(At 4th and 12th weeks)

研究者

发起方
Laboratorios Ordesa
申办方类型
Industry
责任方
Sponsor

研究点 (3)

Loading locations...

相似试验