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临床试验/NCT01235884
NCT01235884已完成不适用

Prevention of the Minor Digestive Disorders by Lactobacillus Reuteri Supplementation.

University of Bari8 个研究点 分布在 1 个国家目标入组 492 人开始时间: 2010年9月1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
492
试验地点
8
主要终点
Reduction of the onset of gaseous colic, regurgitation and of constipation.

研究概览

简要总结

Aim of the study. To evaluate if L. reuteri DSM 17938 supplementation since the first days of life can reduce the onset of gaseous colic in neonates and the onset of minor digestive disorders such as regurgitation and constipation.

Study Design. Double blind, randomized, controlled, multicenter study. 492 neonates of 37-42 gestational age, breast or formula fed, will receive L. reuteri 5 drops (1x108 CFU) daily or placebo for 28 days.

After the inclusion, at baseline will be performed :

  • Paediatric visit
  • antropometric valutation
  • number of the daily crying minutes, number of regurgitation and number of daily evacuation

The patients will receive the probiotics/placebo every days for 28 days and the 29th will be repeated the following analyses:

  • Paediatric visit
  • antropometric valutation
  • number of daily crying minutes
  • numbers of regurgitation
  • numbers of evacuations

Primary outcome :

To define if Lactobacillus reuteri supplementation can reduce the onset of gaseous colic, regurgitation and of constipation.

Inclusion criteria

  • neonates of 37-42 week gestational age and appropriate birth weight
  • Recruitment age: until 7 days of life
  • Informed consent signed

Exclusion criteria

  • Presence of other gastrointestinal diseases.
  • Use of FANS, aspirin or other drugs
  • Use of antibiotics and/or PPIs e/o anti-H2
  • Participation to other clinical trials

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 (Participant, Investigator)

入排标准

年龄范围
1 Day 至 7 Days(Child)
性别
All
接受健康志愿者

入选标准

  • neonates of 37-42 week gestational age and appropriate birth weight
  • Recruitment age: until 7 days of life
  • Informed consent signed

排除标准

  • Presence of other gastrointestinal diseases.
  • Use of FANS, aspirin or other drugs
  • Use of antibiotics and/or PPIs e/o anti-H2
  • Participation to other clinical trials

结局指标

主要结局

Reduction of the onset of gaseous colic, regurgitation and of constipation.

时间窗: one year

After the inclusion, at baseline will be performed : * Paediatric visit * antropometric valutation * number of the daily crying minutes, number of regurgitation and number of daily evacuation The patients will receive the probiotics/placebo every days for 28 days and the 29th will be repeated the following analyses: * Paediatric visit * antropometric valutation * number of daily crying minutes * numbers of regurgitation * numbers of evacuations

次要结局

未报告次要终点

研究者

发起方
University of Bari
申办方类型
Other
责任方
Principal Investigator
主要研究者

Flavia Indrio

Senior Consultant Neonatologist Pediatric Gastroenterologist

University of Bari

研究点 (8)

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