Prevention of the Minor Digestive Disorders by Lactobacillus Reuteri Supplementation.
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
- 是
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
Flavia Indrio
Senior Consultant Neonatologist Pediatric Gastroenterologist
University of Bari
