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临床试验/NCT02430831
NCT02430831Unknown4 期

Randomized Controlled Trial Testing the Effect of Milk Formula Supplemented With L. Reuteri on Crying Time in Colicky Infants Less Than 3 Months Old

University of Bari1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2015年5月1日最近更新:
适应症

试验速览

阶段
4 期
发起方
入组人数
60
试验地点
1
主要终点
Daily Crying duration

研究概览

简要总结

Study type:

Randomized controlled trial with two parallel arms Objectives

Primary : Demonstrate that daily supplementation of colicky infants with Nidina formula containing L. reuteri DSM 17938 decreases the daily crying duration at 21 days Secondary : Evaluate the effects of daily supplementation of colicky infants with Nidina formula containing L. reuteri DSM 17938 measured as

  1. the number of "responders" or the "treatment success" (ie infants for which defined as the percentage of children achieving a reduction in the daily average crying time >50% in 3 weeks. (day 1 to day 21 of the study)
  2. maternal depression and family functioning scoring

详细描述

Inclusion criteria :

  • less then 12 weeks of age
  • term infant (≥ 38 weeks gestational age)
  • birth weight > 2,500g
  • infantile colic diagnosed according to modified Wessel's criteria, i.e. crying more than an average of 180 min/day during the 3 days prior to enrollment.
  • parental motivation to postpone changes in the infant feeding mode, unless necessary

Exclusion criteria:

  • birth weight less than 2500 g
  • failure to thrive
  • chronic illness or major medical problem
  • gastrointestinal disease
  • cow's milk allergy ( confirmed prior to exclusion; difficult to diagnose so early ??)
  • use of any antibiotic or probiotic in the week (7 days) prior to enrollment
  • use of proton pump inhibitors in the week (7 days) prior to enrollment
  • if breastfeeding, use of probiotic by the mother in the week (7 days) prior to enrollment
  • infant receiving solid foods (such as cereals, mashed fruits or vegetable purée)
  • change of feeding mode planned by parents during the study period

Randomization and blinding: to be written by the CRO, according to its own procedures.

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
— 至 12 Weeks(Child)
性别
All
接受健康志愿者

入选标准

  • Inclusion criteria :
  • less then 12 weeks of age
  • term infant (≥ 38 weeks gestational age)
  • birth weight > 2,500g
  • infantile colic diagnosed according to modified Wessel's criteria, i.e. crying more than an average of 180 min/day during the 3 days prior to enrollment.
  • parental motivation to postpone changes in the infant feeding mode, unles

排除标准

  • - birth weight less than 2500 g
  • failure to thrive
  • chronic illness or major medical problem
  • gastrointestinal disease
  • cow's milk allergy ( confirmed prior to exclusion; difficult to diagnose so early ??)
  • use of any antibiotic or probiotic in the week (7 days) prior to enrollment
  • use of proton pump inhibitors in the week (7 days) prior to enrollment
  • if breastfeeding, use of probiotic by the mother in the week (7 days) prior to enrollment
  • infant receiving solid foods (such as cereals, mashed fruits or vegetable purée)
  • change of feeding mode planned by parents during the study period

结局指标

主要结局

Daily Crying duration

时间窗: three days

The average crying time in minutes per day measured on day 19, 20, and 21 between active and placebo groups.

次要结局

  • Mother depression (mother depression Scale)(One day)
  • Rate of success (decrease in mean daily crying time)(3 days)
  • Family functional score (family functioning scale)(one day)

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

MD

University of Bari

研究点 (1)

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