Clinical Trial of L. Reuteri in Infantile Colic 2017

Last updated: July 27, 2019
Sponsor: Innovacion y Desarrollo de Estrategias en Salud
Overall Status: Active - Recruiting

Phase

N/A

Condition

Colic

Treatment

N/A

Clinical Study ID

NCT03360253
Colic2017
  • Ages < 9
  • All Genders

Study Summary

RCT to evaluate the safety and efficacy of Lactobacillus reuteri DSM 17938 to significantly reduce the duration of crying time and fussines in infants from 15days to 4 months of age with colic, feed with human milk (30% sample) or infant formula (70%)

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Younger than 10 weeks of age

  • Full term infant (37-42 weeks gestational age)

  • Birth weight ≥ 2,500g

  • Apgar score ≥ 7 at 5 minutes

  • Infantile colic diagnosed according to modified Wessel's criteria (crying more than 180 min/day during 3 days for at least a week prior to enrolment)

  • Parental motivation to postpone changes in the infant feeding mode, unless necessary

  • Stated availability throughout the study period

  • Parent(s) willingness and ability to fill out charts and questionnaires

  • Signed informed consent

Exclusion

Exclusion Criteria:

  • Failure to thrive

  • Chronic illness or major medical problem

  • Gastrointestinal disease

  • Use of any antibiotic 2 weeks before Day 1 in the study. This applies also tolactating mothers whose infants participate in the trial

  • Use of supplements/eaten foods that contain Lactobacillus reuteri, 2 weeks before Day 1

  • Use of proton pump inhibitors in the week (7 days) prior to enrolment

  • If breastfeeding, use of probiotic by the mother in the week (7 days) prior toenrolment and throughout the study period

  • Use of infant formula with hydrolysed protein

  • Infant receiving solid foods (such as cereals, mashed fruits or vegetable purée)

  • Change of feeding mode planned by parents during the study period

Study Design

Total Participants: 244
Study Start date:
January 01, 2018
Estimated Completion Date:
January 30, 2020

Study Description

RCT to evaluate the safety and efficacy of Lactobacillus reuteri DSM 17938 administrated for 21 days to significantly reduce the duration of crying time and fussines in infants from 15days to 4 months of age with colic. 66 infants feed with human milk and 180 infant feed with infant formula will be included. As primary outcome we will measure the difference between children receiving L. reuteri DSM 17938, 108 CFU vs children receiving placebo regarding average daily crying duration (minutes per day, from average of crying from days 19 to 21 after randomization), measured by Barr diary. Secondary/exploratory outcomes will be average of crying time on day 7 and 14 (Barr diary) of L. reuteri groups vs placebo group; average of crying and fussing time on day 7, 14 and average from days 19 to 21 after randomization (Barr diary) of L. reuteri groups vs placebo group; responders percentage on day 7, 14 and 21, decrease in daily average crying time of 50% during the study; QoL (PedsQL-2.0-Family Impact Module AU2.0 spa-MX) changes from baseline to days 7, 14 and 21 and Edinburg postnatal depression scale for mothers from baseline to days 7, 14 and 21

Connect with a study center

  • Hospital General Dr. Manuel Gea Gonzalez

    Mexico city, Tlalpan 14080
    Mexico

    Active - Recruiting

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