search
Back to results

Evaluation of Lactobacillus Reuteri DSM 17938 + Vitamin D3 in the Prevention of RRI in Paediatric Patients (LR_D3)

Primary Purpose

Recurrent Respiratory Tract Infections

Status
Terminated
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Lactobacillus reuteri DSM 17938 + Vitamine D3
Placebo
Sponsored by
Noos S.r.l.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Recurrent Respiratory Tract Infections focused on measuring RRI, probiotics, vitamin D3, L. reuteri

Eligibility Criteria

1 Year - 6 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Patients between 1 and 6 years of age at the enrollment; both sexes
  • Patients with an history of RRI, according to the definition (The definition of Recurrent respiratory infections (RRI) is the onset of 8 or more documented airway infections during the year, in preschool children (up to three years of age) or 6 or more in children older 3 years, in the absence of any other underlying pathological condition) in the previous year.
  • Atopic and non-atopic patients
  • Willing and able to give informed consent of participation in the study by parent or legal guardian.

Exclusion Criteria:

  • Presence of autoimmune diseases, immunodeficiency, neuromuscular diseases, congenital cardiomyopathies, metabolic diseases
  • Patients in therapy with other drugs for the treatment of RRI
  • Supplementation with probiotics and /or prebiotics in the previous 2 weeks
  • Vitamin D intake in the last 4 weeks
  • IgA deficiency
  • Antibiotic treatment at least 4 week before in inclusion
  • Participation in other clinical trials

Sites / Locations

  • University of Campania Luigi Vanvitelli

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Reuterin D3

Placebo

Arm Description

Patients should take 10 drops once a day during meals for 4 months followed by 2 months of follow up.

Patients should take 10 drops once a day during meals for 4 months followed by 2 months of follow up.

Outcomes

Primary Outcome Measures

Change of the number of respiratory infection
Change of the number of respiratory infection respect the previous year

Secondary Outcome Measures

Change of number of days with fever
To evaluate the change of the number of days with fever
Change of the antibiotic use
To evaluate the change of the antibiotic use
Change of number of visit to Pediatrician
To evaluate the change of the number of visit to Pediatrician
Change of number of days of absence from the nursery / kindergarten
To evaluate the change of the number of days of absence from the nursery / kindergarten
Changes of days of absence from work by parents
To evaluate the change of days of absence from work by parents
Modification of intestinal microflora
To evaluate the modification of intestinal microflora

Full Information

First Posted
May 25, 2020
Last Updated
March 21, 2023
Sponsor
Noos S.r.l.
search

1. Study Identification

Unique Protocol Identification Number
NCT04408443
Brief Title
Evaluation of Lactobacillus Reuteri DSM 17938 + Vitamin D3 in the Prevention of RRI in Paediatric Patients
Acronym
LR_D3
Official Title
Evaluation of a Food Supplement Containing Lactobacillus Reuteri DSM 17938 + Vitamin D3 in the Prevention of Recurrent Respiratory Infections in Paediatric Patients
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Terminated
Why Stopped
No enrollment due COVID PANDEMIA
Study Start Date
November 25, 2019 (Actual)
Primary Completion Date
September 30, 2021 (Actual)
Study Completion Date
September 30, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Noos S.r.l.

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of this protocol is to evaluate, in a multicenter, randomized, double blind vs placebo clinical trial the effects of a marketed food supplement containing Lactobacillus reuteri DSM 17938 and vitamin D3 (Reuterin® D3) in the prevention of recurrent respiratory infections in pediatric patients suffered from Recurrent Respiratory Infection (RRI) in previous years.
Detailed Description
Several clinical trials documented the efficacy of probiotics in the prevention and treatment of acute gastroenteritis, while there is little evidence on the efficacy of the probiotics in the prevention of children respiratory infections. The biological activity of probiotics is linked, partly, to their capacity to adhere to enterocytes. This would avoid the binding of pathogenic bacteria through a competitive exclusion mechanism. This inhibition toward pathogen bacteria on epithelial and mucosal level (substrate), thanks also to the production of antimicrobial substances, can have a beneficial effect on the balance of the intestinal microflora of the host and improve its immunity. The adhesion of probiotic bacteria to the enterocyte membrane receptors influences the activation of second messengers that induces the production of cytokines. The presence of probiotic bacteria influences the commensal microorganisms in the production of lactic acid and bacteriocins. These substances inhibit the growth of pathogens and modify the balance of commensal bacteria of the intestinal bacterial flora. Numerous controlled clinical trials show that L. reuteri DSM 17938 colonizes the human gastric and intestinal epithelium and modulates the immune response, particularly through CD4 + T-helper cells in the ileum. These data confirm the pre-clinical evidence obtained in animal models; furthermore these immunomodulatory effects may explain some clinical properties of L. reuteri DSM 17938 such as the prevention of diarrhea, inhibition of pathogen infectionand the following immune system response of the host to these pathogens, as well as the potential modulation of the immune response by the Th1/Th2 balance in the human intestinal epithelium, an answer that has been linked to the prevention and treatment of allergy. In a recent, randomized, double-blind, placebo-controlled clinical trial, L. reuteri DSM 17938, supplemented for three months to healthy children aged 6-36 months attending nursery schools, demonstrated not only a significant reduction of episodes and duration of diarrhea but also of respiratory tract infections with consequent reduction of costs for society. Despite the prevalence of food with vitamin D and multivitamin products, reports regarding non-optimal vitamin D levels in adults and children in the world have increased, in particular among those subjects overweight and with dark pigmentation of the skin. In addition to its well-known effects on bone health, vitamin D is indeed an important immune regulator, because it stimulates innate immunity and modulates inflammation. An analysis of data from the National Health and Nutrition Examination Survey (NHANES) between 1988 and 1994 showed an inverse relationship between vitamin D levels and the incidence of upper respiratory tract infections (URTI). These results were supported by other studies showing an increased risk of acute lower respiratory tract infections in subjects with low levels of vitamin D. Historically, the association between rickets and the risk of serious respiratory infections is well known and vitamin D deficiency has been associated with an increased risk to contract the flu. These considerations have led to the hypothesis that supplementation with a probiotic added with vitamin D3 may influence the composition of intestinal flora by improving the immune system and therefore reducing episodes of respiratory infections, particularly frequent during preschool age.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Recurrent Respiratory Tract Infections
Keywords
RRI, probiotics, vitamin D3, L. reuteri

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Masking Description
Triple (Participant, Care Provider, Investigator)
Allocation
Randomized
Enrollment
200 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Reuterin D3
Arm Type
Active Comparator
Arm Description
Patients should take 10 drops once a day during meals for 4 months followed by 2 months of follow up.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Patients should take 10 drops once a day during meals for 4 months followed by 2 months of follow up.
Intervention Type
Dietary Supplement
Intervention Name(s)
Lactobacillus reuteri DSM 17938 + Vitamine D3
Intervention Description
Lactobacillus reuteri DSM 17938 (10E8 CFU in 5 drops), Vitamin D3 (400 IU in 5 drops), sunflower oil, medium chain triglycerides, silicon dioxide
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
sunflower oil, medium chain triglycerides, silicon dioxide
Primary Outcome Measure Information:
Title
Change of the number of respiratory infection
Description
Change of the number of respiratory infection respect the previous year
Time Frame
4 months + 2 months of follow up
Secondary Outcome Measure Information:
Title
Change of number of days with fever
Description
To evaluate the change of the number of days with fever
Time Frame
4 months + 2 months of follow up
Title
Change of the antibiotic use
Description
To evaluate the change of the antibiotic use
Time Frame
4 months + 2 months of follow up
Title
Change of number of visit to Pediatrician
Description
To evaluate the change of the number of visit to Pediatrician
Time Frame
4 months + 2 months of follow up
Title
Change of number of days of absence from the nursery / kindergarten
Description
To evaluate the change of the number of days of absence from the nursery / kindergarten
Time Frame
4 months + 2 months of follow up
Title
Changes of days of absence from work by parents
Description
To evaluate the change of days of absence from work by parents
Time Frame
4 months + 2 months of follow up
Title
Modification of intestinal microflora
Description
To evaluate the modification of intestinal microflora
Time Frame
4 months + 2 months of follow up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Year
Maximum Age & Unit of Time
6 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Patients between 1 and 6 years of age at the enrollment; both sexes Patients with an history of RRI, according to the definition (The definition of Recurrent respiratory infections (RRI) is the onset of 8 or more documented airway infections during the year, in preschool children (up to three years of age) or 6 or more in children older 3 years, in the absence of any other underlying pathological condition) in the previous year. Atopic and non-atopic patients Willing and able to give informed consent of participation in the study by parent or legal guardian. Exclusion Criteria: Presence of autoimmune diseases, immunodeficiency, neuromuscular diseases, congenital cardiomyopathies, metabolic diseases Patients in therapy with other drugs for the treatment of RRI Supplementation with probiotics and /or prebiotics in the previous 2 weeks Vitamin D intake in the last 4 weeks IgA deficiency Antibiotic treatment at least 4 week before in inclusion Participation in other clinical trials
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michele Miraglia del Giudice, Prof.
Organizational Affiliation
University of Campania "Luigi Vanvitelli"
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Campania Luigi Vanvitelli
City
Naples
ZIP/Postal Code
80138
Country
Italy

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Evaluation of Lactobacillus Reuteri DSM 17938 + Vitamin D3 in the Prevention of RRI in Paediatric Patients

We'll reach out to this number within 24 hrs