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Bifidobacterium Animalis Subsp. Lactis for Lowering the Risk of Common Infections in Hospitalized Children (PROBIC II)

Primary Purpose

Gastrointestinal Tract Infections, Respiratory Tract Infections

Status
Completed
Phase
Not Applicable
Locations
Croatia
Study Type
Interventional
Intervention
Bifidobacterium animalis subsp. lactis
Sponsored by
Children's Hospital Zagreb
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Gastrointestinal Tract Infections

Eligibility Criteria

1 Year - 18 Years (Child, Adult)All Sexes

Inclusion Criteria:

  • Children hospitalized at the Department of Paediatrics, Children's Hospital Zagreb
  • Age from 1 year to 18 years
  • Signed informed consent by the parents

Exclusion Criteria:

  • Immunodeficiency
  • Infants from neonatal period until 1 year of age
  • Re-hospitalisation (readmission in a hospital within one month)
  • Receiving probiotic and /or prebiotic products prior to enrolment (2 weeks prior to hospitalization)
  • Neoplasms
  • Severe chronic diseases
  • Hospitalization shorter than 3 days

Sites / Locations

  • Children's Hospital Zagreb

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Bifidobacterium animalis subsp. lactis

Placebo

Arm Description

Outcomes

Primary Outcome Measures

Common infections in children
Number of children with common infections (gastrointestinal and respiratory infections): Gastrointestinal tract infections defined as diarrhoea (3 or more loose or watery stools in 24 hours or increase of number of stools for more than 50% in 24 hours) or vomiting (defined by physician and not a result of other symptoms including cough or diseases including gastroesophageal reflux disease or neurological conditions) or both. Respiratory tract infections defined as: pharyngitis, otitis, common cold, pneumonia, bronchitis and bronciolitis (all infections diagnosed by physician) Number of children with adverse events.

Secondary Outcome Measures

Duration of symptoms
Duration of symptoms in days

Full Information

First Posted
October 3, 2012
Last Updated
July 24, 2013
Sponsor
Children's Hospital Zagreb
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1. Study Identification

Unique Protocol Identification Number
NCT01702766
Brief Title
Bifidobacterium Animalis Subsp. Lactis for Lowering the Risk of Common Infections in Hospitalized Children
Acronym
PROBIC II
Study Type
Interventional

2. Study Status

Record Verification Date
July 2013
Overall Recruitment Status
Completed
Study Start Date
December 2012 (undefined)
Primary Completion Date
July 2013 (Actual)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Children's Hospital Zagreb

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Hypothesis: Use of Bifidobacterium animalis subsp. lactis can effectively prevent common nosocomial (gastrointestinal and respiratory) infections. Nosocomial infection will be defined as infections which develop more than 48 hours after admission and they are not present or incubating on admission This study is a prospective, randomized, double blind, placebo- controlled parallel study in children hospitalized at Children's hospital Zagreb. The study will investigate the effect of supplementation with the probiotic strain Bifidobacterium animalis subsp. lactis on the incidence and duration of gastrointestinal and respiratory infections. The test product is a sachet containing 1 gram of powder. The test product will contain minimum 1 billion CFU (colony forming units) probiotic per serving. The placebo product is an identical product except for the absence of probiotics. The study includes an intervention period lasting the length of the hospital stay. The study product will be consumed daily in the morning together with breakfast. The consumption of the study products will be taken under the surveillance of the physician. Data on infections will be diagnosed by a physician and recorded in a CRF. The incidence of infections will be analyzed based on the information recorded in the CRF.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gastrointestinal Tract Infections, Respiratory Tract Infections

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment

8. Arms, Groups, and Interventions

Arm Title
Bifidobacterium animalis subsp. lactis
Arm Type
Active Comparator
Arm Title
Placebo
Arm Type
Placebo Comparator
Intervention Type
Dietary Supplement
Intervention Name(s)
Bifidobacterium animalis subsp. lactis
Primary Outcome Measure Information:
Title
Common infections in children
Description
Number of children with common infections (gastrointestinal and respiratory infections): Gastrointestinal tract infections defined as diarrhoea (3 or more loose or watery stools in 24 hours or increase of number of stools for more than 50% in 24 hours) or vomiting (defined by physician and not a result of other symptoms including cough or diseases including gastroesophageal reflux disease or neurological conditions) or both. Respiratory tract infections defined as: pharyngitis, otitis, common cold, pneumonia, bronchitis and bronciolitis (all infections diagnosed by physician) Number of children with adverse events.
Secondary Outcome Measure Information:
Title
Duration of symptoms
Description
Duration of symptoms in days
Other Pre-specified Outcome Measures:
Title
Severity of infection
Description
Severity of GI infections based on Vesikari scale Severity of respiratory infections according to the physician based on visual analogue scale

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Year
Maximum Age & Unit of Time
18 Years
Eligibility Criteria
Inclusion Criteria: Children hospitalized at the Department of Paediatrics, Children's Hospital Zagreb Age from 1 year to 18 years Signed informed consent by the parents Exclusion Criteria: Immunodeficiency Infants from neonatal period until 1 year of age Re-hospitalisation (readmission in a hospital within one month) Receiving probiotic and /or prebiotic products prior to enrolment (2 weeks prior to hospitalization) Neoplasms Severe chronic diseases Hospitalization shorter than 3 days
Facility Information:
Facility Name
Children's Hospital Zagreb
City
Zagreb
ZIP/Postal Code
10000
Country
Croatia

12. IPD Sharing Statement

Citations:
PubMed Identifier
25733653
Citation
Hojsak I, Tokic Pivac V, Mocic Pavic A, Pasini AM, Kolacek S. Bifidobacterium animalis subsp. lactis fails to prevent common infections in hospitalized children: a randomized, double-blind, placebo-controlled study. Am J Clin Nutr. 2015 Mar;101(3):680-4. doi: 10.3945/ajcn.114.102004. Epub 2015 Jan 7.
Results Reference
derived

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Bifidobacterium Animalis Subsp. Lactis for Lowering the Risk of Common Infections in Hospitalized Children

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