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Impact of Probiotic Preparation VSL#3 on Infants Colics

Phase 4
Conditions
Infant Colics
Interventions
Dietary Supplement: VSL#3 drops
Dietary Supplement: VSL#3 drops placebo
Registration Number
NCT01869426
Lead Sponsor
Policlinico Hospital
Brief Summary

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.

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.

Detailed Description

Aim of the study is to evaluate the improvement of colics symptoms by the oral administration of VSL#3 and the difference in the daily average crying time (measured with parental diary) between end of treatment and baseline.

In this study, 62 infants will be enrolled and will receive 10 drops per day of VSL#3 or Placebo according to randomization list. The study product will be supplied as a box containing the oil bottle and a powder stick. The product should be stored refrigerated. On the first day of supplementation, the mother will open the sachet, pour the contents into the bottle and shake vigorously. A dropper is provided to count the drops. The suspension must be shaken vigorously before every use. Compliance will be monitored by filling out a diary.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
62
Inclusion Criteria
  • Infants aged between 30 and 90 days
  • Breast fed exclusively during length of trial
  • Diagnosis of infantile colic according to Wessel's criteria i.e paroxysmal fussing in infancy for more than three hours per day, at least three days per week but not treated previously for colics.
  • Debut of colic symptoms 6+/-1 days before randomization
  • Written informed consent from one or both parents
  • Stated availability and reliability throughout the study period.
Exclusion Criteria
  • Major chronic disease
  • Gastrointestinal disease
  • Administration of antibiotics the week before randomization
  • Administration of probiotics two weeks before randomization
  • Infants with GI malformation, cystic fibrosis, other genetic diseases
  • Participation in other clinical trials.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
VSL#3 dropsVSL#3 drops31 infants will receive 10 drops active product that should be taken daily (preferably in the morning before feeding) for 21 days.
VSL#3 drops placeboVSL#3 drops placebo31 infants will receive 10 drops of placebo product that should be taken daily (preferably in the morning before feeding) for 21 days.
Primary Outcome Measures
NameTimeMethod
Improvement of colics symptoms3 weeks

improvement of colics symptoms by the oral administration of probiotic VSL#3 drops

Secondary Outcome Measures
NameTimeMethod
Difference in the daily average crying time between end of treatment and baseline.3 weeks

Difference in the daily average crying time, measured with parental diary, between end of treatment and baseline.

Trial Locations

Locations (1)

Dept Of Obstetrics and Neonatology - Section of Neonatology University of Bari Policlinico Hospital

🇮🇹

Bari, Italy

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