跳至主要内容
临床试验/NCT02839239
NCT02839239已完成不适用

Role of Lactobacillus Rhamnosus (FloraActive™) 19070 and Lactobacillus Reuteri (FloraActive™) DSM 12246 in Infant Colic: a Controlled Dietary Study

Biocare Copenhagen A/S0 个研究点目标入组 168 人开始时间: 2016年12月9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
168
主要终点
Change in mean cry/fuss time (min/day) from day 0 through day 28

研究概览

简要总结

The objective of this study is to determine an efficacy of the combination of L. rhamnosus 19070-2 (FloraActiveTM) and L. reuteri DSM 122460 (FloraActiveTM) in decreasing cry/fuss in infants aged 4 through 12 weeks with IC. The active group of infants will receive lactobacilli with vitamin D3 while the control group will receive vitamin D3 2 times daily as oil suspension for 28 days. Duration of infant fuss/cry will be measured at baseline and at the end of intervention to define a difference between the groups

详细描述

There is accumulating interest in role of lactobacilli in decreasing cry and fuss in infant colic, the condition that affects around 1 of 4-5 infants. The interest for dietary supplementation has been evoked by a line of earlier studies, indicating that infants with colic had an increased number of gas-forming E.coli in the intestines and potential interference between lactobacilli and E.coli. Systematic review of evidence, based on the 6 randomized controlled dietary studies, conducted in Italy, Poland, Australia, Canada, and Finland, has concluded of the decrease of the mean time cry of infant by -55 minutes a day after the 3 weeks dietary course with lactobacilli . In the mentioned studies most commonly used lactobacilli were L. reuteri, however, the effect of combination of L. reuteri with other lactobacilli remains unknown.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
4 Weeks 至 12 Weeks(Child)
性别
All
接受健康志愿者

入选标准

  • Informed consent form signed by both parents.
  • Gender: males and females;
  • Age: 4 -12 weeks;
  • Infant colic, defined as cry/fussing lasting > 3 h, occurring > 3 d for 7 days;
  • Gestational age 37-42 weeks;
  • Birth weight 2,500-4,200 g;
  • Stated availability throughout the study period;
  • Sated availability of mobile phone or phone with answering machine.

排除标准

  • Any formula feeding in any amount;
  • Failure to thrive (weight gain less than 100 grams per week as averaged from the birth weight to the weight at entry);
  • Current maternal smoking;
  • Known moderate or severe disease of any systems (neural, skeletal, muscular, cutaneous, gastrointestinal, respiratory, genital, urinary, immune);
  • Present intake of antibiotics by infant or mother;
  • Present intake of prebiotics or probiotics by infant or mother;
  • Difficulty of parents to comprehend study requirements as judged by the physician;
  • Suspected parental alcohol or drug addiction as judged by the physician.

研究组 & 干预措施

Drops with lactobacilli and vitamin D3

Experimental

Exclusive breast feeding plus L. rhamnosus 19070-2 and L. reuteri DSM 12246 in a dose of 125 x 106 CFU (both strains) with 1,667 mg fructooligosaccharides and 2,5 mcg (100 IU) vitamin D3 (in sunflower oil) per 6 drops. One dose (6 drops) in the first morning (from 6 AM) breastfeeding, and one dose (6 drops) in one of the evening (6 PM-12 PM) breast feedings for 28 days.

干预措施: Drops with lactobacilli and vitamin D3 (Dietary Supplement)

Drops with vitamin D3

Placebo Comparator

Exclusive breast feeding plus 2.5 mcg (100 IU) vitamin D3 (in sunflower oil) per 6 drops. One dose (6 drops) in the first morning (from 6 AM) breastfeeding, and one dose (6 drops) in one of the evening (6 PM-12 PM) breast feedings for 28 days.

干预措施: Drops with vitamin D3 (Dietary Supplement)

结局指标

主要结局

Change in mean cry/fuss time (min/day) from day 0 through day 28

时间窗: 28 days

Change in mean cry/fuss time

次要结局

  • Recovery success (percent) at 7, 14, 21, 28 days, defined as reduction in duration of cry time less than 3 hours per day (unmet Wessel criteria);(7, 14, 21, 28 days)
  • Cry and fuss time (min/day) on days 0, 7, 14, 21, 28(7, 14, 21, 28 days)
  • Change in mean cry time (min/day) from day 0 through day 28(28 days)
  • Change in mean fuss time (min/day) from day 0 through day 28(28 days)
  • Treatment success (percent) at 7, 14, 21, 28 days, defined as more than 25% and 50% reduction in cry time from baseline(7, 14, 21, 28 days)

研究者

发起方
Biocare Copenhagen A/S
申办方类型
Industry
责任方
Sponsor

相似试验