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Completed

NCT Number: NCT05484102

Preventive Effect of Cow's Milk Fermented With Lactobacillus Paracasei CBA L74 on Common Infectious Diseases in Children

this is a double-blind randomized placebo controlled clinical trial. 200 healthy children aged 12-48 months, attending day care or preschool for at least 5 days a week, regularly checked by the family pediatrician (FP) involved in the trial, were considered for the study and consecutively contacted during scheduled medical examinations at the FPs office. study plan is 3-month treatment period. The clinical evaluation will be carried out at enrollment, at 30, 60 and 90 days from the beginning of the treatment by the pediatrician. fecal and nasal mucus samples for immunological and microbiological analysis will be collected before the treatment and at 90 days (end of treatment).

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Key information

Age range

12 month–48 month

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Clinica Pediatrica

Bari, Apulia, 70125, Italy

About this study

Subjects were supplemented daily for 3 months with cow's skim milk fermented with L. paracasei CBA L74 (group A) or placebo (group B).Enrolled children will be randomly assigned, with the use of a computer-generated randomization list to receive either milk fermented with Lactobacillus paracasei CBA L74 or placebo once. Placebo and fermented milk had the same shape, the placebo's taste, dimension, indication, and appearance. At enrollment the family pediatricians consulted the clinical records of each child for previous diseases and pharmacological treatments. At the baseline, after obtaining informed consent from the parents/tutors of each child, the health status of all the study subjects was carefully assessed, and the presence of infectious diseases or other disease was ruled out by means of a complete physical examination, including vital signs (body temperature, pulse rate, respiration rate, blood pressure); neurological status; body growth status; nutritional status; hydration; skin evaluation; otoscopy; evaluation of oral cavity; respiratory/abdomen/lymphonode examination; and genital examination.

A diary will be given to the parents; on a daily basis, patients will monitor and record the frequency/severity of symptoms, episodes of respiratory and/or gastrointestinal infection and their duration and school absence on the diary.

Fecal Analysis: three fecal samples for microbiological and immunological analysis will be collected before treatment and at 90 days (end of treatment). Nasal mucus samples for immunological analysis will be collected before the treatment and at 90 days (end of the treatment).

The study was approved by the Ethics Committee of the Universities of Bari.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Healthy children aged 12-48 months
  • attending day care or preschool for at least 5 days a week

Exclusion criteria

The exclusion criteria were:

  • age <12 months or >48 months
  • concomitant chronic infections, chronic systemic diseases, chronic inflammatory bowel diseases, autoimmune diseases, immunodeficiency, malignancy, metabolic diseases
  • chronic respiratory tract diseases including respiratory allergies and cystic fibrosis
  • malformations of gastrointestinal or urinary or respiratory tract
  • history of respiratory or gastrointestinal or urinary tract surgery
  • congenital cardiac defects
  • functional bowel disorders
  • suspected or challenge-proved food allergy, food intolerances
  • severe malnutrition (z-score for weight-for-height <3 standard deviation scores)
  • use of antibiotics or pre/pro/synbiotics or immune stimulating products in the 2 weeks before the enrolment
  • Siblings of subjects enrolled in the study were not allowed to participate to the trial.

Treatment and study plan

milk fermented with lactobacillus paracasei CBA L74

Dietary Supplement

milk fermented with lactobacillus paracasei CBA L74 will be administered daily for 3 months to 100 children. Participants were supplied with the milk product in powder form, by Heinz Italia SpA, Segrate, Italy. The study products were provided in tins containing 400 g of powder, and the packaging was similar and the tins were stored at room temperature in a dry environment. The family pediatricians instructed parents about the daily amount of the assigned study product and the method of preparation. All subjects received 7 g/day of study products diluted in a maximum of 150 mL of cow's milk or water. After dilution, the look and the taste were the same for all of the study products.

placebo milk formula

Dietary Supplement

placebo milk formula containing maltodextrins will be administered daily for 3 months to 100 children. The study products were provided in tins containing 400 g of powder, and the packaging was similar and the tins were stored at room temperature in a dry environment. The family pediatricians instructed parents about the daily amount of the assigned study product and the method of preparation. All subjects received 7 g/day of study products diluted in a maximum of 150 mL of cow's milk or water. After dilution, the look and the taste were the same for all of the study products.

Primary outcomes

  1. preventive effect of cow's milk fermented with Lactobacillus paracasei CBA L74 on common infectious disease

    Time frame: 3 months

    the rate of children experiencing at least one episode of common infectious disease

Secondary outcomes

  1. Total number of common infectious disease

    Time frame: 3 months

    evaluate the total number of common infectious disease

  2. use of medications

    Time frame: 3 months

    use of medications (antibiotics, antipyretics, steroids)

  3. emergency department medical examinations and hospitalizations

    Time frame: 3 months

    access to emergency department medical examinations and hospitalizations

  4. days of work lost by the parents

    Time frame: 3 months

    evaluation of days of work lost by the parents

  5. days of school lost by the children

    Time frame: 3 months

    evaluation of days of school lost by the children

Sponsors and collaborators

Lead sponsor

University of Bari

Other

Collaborators

  • Heinz Italia SpA

Registry information

Official study title

Preventive Effect of Cow's Milk Fermented With Lactobacillus Paracasei CBA L74 on Upper Respiratory Tract and Gastrointestinal Infectious Diseases in Children: a Double-blind, Randomized, Placebo-controlled Trial

Acronym: FERCT19

Important dates

Study start
2022
Primary completion
2024
Study completion
2024
First posted
Aug 2, 2022
Registry last updated
Sep 19, 2024

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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