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Completed

NCT Number: NCT01541046

Lactobacillus Reuteri DSM 17938 Versus Placebo in the Treatment of Infantile Colic

Infantile colic is a common medical condition which remains a frustrating problem for parents and health care providers with no clear treatment guidelines. To fill the void in existing literature, we present a protocol to examine whether probiotics are effective in decreasing infantile colic symptoms when compared to placebo treatment.

We hypothesize that oral administration of the probiotic L. reuteri DSM 17938 will reduce symptoms of infantile colic in breastfed infants in comparison to placebo.

An interim analysis will be conducted after 50 infants randomized to monitor both safety and efficacy.

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Key information

Age range

21 day–180 day

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

The Hospital for Sick Children

Toronto, Ontario, M5V1X8, Canada

About this study

Infantile colic is one of the most commonly reported medical problems within the first three months of life causing appreciable distress for both parents and pediatricians. The reported incidence of infantile colic ranges from 3% to 28% in prospective studies and up to 40% in retrospective surveys.

The pathogenesis of infantile colic remains elusive despite decades of research. It appears that multiple independent origins might be involved: amongst them infant's difficult temperament, inadequate mother-infant communication or maternal anxiety, transient lactase deficiency, exposure to cow's milk, abnormal gastrointestinal function, maternal smoking during pregnancy or after delivery. Consequently, various treatment approaches have been tried to alleviate this condition.

Recent studies have suggested that changes of intestinal microflora of a newborn may play an important role in pathogenesis of infantile colic. Therefore, dietary supplementation with probiotics has been proposed for the improvement of this condition.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Healthy term infant 21-90 days of age
  • Birth weight ≥2500 g
  • Exclusively breastfed (to reduce variability in the intestinal microflora attributable to dietary variations)
  • With colic symptoms (>3 hours of crying on >3 days per week) with debut 10 ± 5 days before enrollment
  • Gestational age between 37 and 42 weeks
  • Apgar score higher than 7 at 5 minutes
  • Written informed consent from a parent

Exclusion criteria

  • Any chronic illness or gastrointestinal disorder as judged by the pediatrician
  • Any history of antibiotic treatment or probiotic supplementation
  • Failure to obtain a written consent by parent/legal guardian
  • Participation in other clinical trials
  • Infants with acute illness
  • Subjects with allergies or family history of allergies to any of the ingredients of the study product or placebo

Treatment and study plan

Biogaia L. reuteri DSM 17938

Biological

Freeze-dried Lactobacillus reuteri DSM 17938 suspended in oil. Brand Name Active Agent: BioGaia™

Probiotic Placebo

Biological

Description of Placebo: contains same excipients as Active Agent, without the active ingredient

Primary outcomes

  1. Mean change in crying time

    Time frame: Baseline, 7 days, 14 days, 21 days

    Reduction of daily median crying time (measured with parental diary) with L. reuteri DSM 17938 versus placebo at any of the time points 7, 14, and 21 days

Secondary outcomes

  1. Number of responders vs. non-responders

    Time frame: Baseline, at 7, 14 and 21 days

    Number of responders versus non-responders with L. reuteri versus placebo at the time points 7, 14, and 21 days. Responder is defined as a decrease in daily average crying time of 50% during the study as measured using the maternal daily diary.

  2. Parental quality of life

    Time frame: Daily for 21 days

    Parental quality of life assessed by self-administered numerical rating scale from 0 (worst possible) to 10 (perfect well-being)

  3. Number of episodes of crying

    Time frame: Over 21 days

    Reduction in the number of episodes of crying (measured with parental diary) with L. reuteri DSM 17938 versus placebo

  4. Duration of episodes of crying

    Time frame: Over 21 days

    Reduction in the duration of episodes of crying (measured with parental diary) with L. reuteri DSM 17938 versus placebo

  5. Changes in stool consistency

    Time frame: Over 21 days

Sponsors and collaborators

Lead sponsor

The Hospital for Sick Children

Other

Registry information

Official study title

Lactobacillus Reuteri DSM 17938 Versus Placebo in the Treatment of Infantile Colic: A Randomized Double-blind Controlled Trial

Important dates

Study start
2011
Primary completion
2014
Study completion
2014
First posted
Feb 29, 2012
Registry last updated
Nov 20, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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