Effects of Lactobacillus Reuteri Plus Vitamin D3 in Children With Atopic Dermatitis
Primary Purpose
Atopic Dermatitis
Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Reuterin D3
Placebo
Sponsored by
About this trial
This is an interventional supportive care trial for Atopic Dermatitis focused on measuring atopic dermatitis, probiotics, vitamin D3, L. reuteri
Eligibility Criteria
Inclusion Criteria:
- diagnosis of atopic dermatitis of mild to moderate grade (SCORAD 25-50)
- signature of the informed consent from both parents or a legal representative
Exclusion Criteria:
- presence of autoimmune diseases, immunodeficiency, inflammatory bowel diseases, cystic fibrosis, metabolic diseases
- use of immunosuppressive drugs and/or systemic corticosteroids in the previous 2 months
- use of antibiotics in the last 4 weeks
- use of probiotics and/or prebiotics in the last 2 weeks
- use of vitamin D in the last 4 weeks
- participation in other clinical trials
Sites / Locations
- Policlinico G.B. Rossi
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 3 months
Patients should take 10 drops once a day during meals for 3 months
Outcomes
Primary Outcome Measures
SCORAD improvement
Improvement of the SCORAD compared to baseline
Secondary Outcome Measures
Vitamin D levels increase
Increase of the levels of Vit. D compared to baseline
LL-37 levels increase
Increase of the levels of cathelicidin compared to baseline
Changes in the fecal microflora
Changes in the fecal microflora compared to baseline
QoL improvement
Improvement of the child's quality of life
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT02945683
Brief Title
Effects of Lactobacillus Reuteri Plus Vitamin D3 in Children With Atopic Dermatitis
Official Title
Randomized Controlled Trial to Evaluate the Beneficial Effects of a Probiotic Food Supplement in Children With Atopic Dermatitis
Study Type
Interventional
2. Study Status
Record Verification Date
March 2023
Overall Recruitment Status
Completed
Study Start Date
February 2015 (Actual)
Primary Completion Date
February 2017 (Actual)
Study Completion Date
February 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Noos S.r.l.
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to evaluate in a randomized, double-blinded, controlled trial, whether a new food supplement containing Lactobacillus reuteri DSM 17938 and vitamin D3 (Reuterin® D3) may improve the SCORAD in pediatric patients with mild to moderate atopic dermatitis
Detailed Description
Recent evidence suggests that childhood allergy development can be linked to an imbalance of the intestinal microbiota. The probiotic bacteria, which contribute to the balance of the intestinal microflora, may play a key role in the modulation of the immune response, looking as a potential resource in the prevention or treatment of allergic disorders.
In this study the investigators will recruit pediatric patients with atopic dermatitis of mild-to-moderate degree, for which the standard treatment consists in using an emollient cream and topical steroids in case of exacerbation.
The investigators assume that participants can receive significant benefits from the addition to their standard treatment of a food supplement containing L. reuteri DSM 17938 and vitamin D3, which, thanks to their beneficial effects on intestinal microbiota and on modulation of the immune response, may compensate for the inadequate capacity of these patients to produce antimicrobial peptides in response to cutaneous aggressions, improving, therefore, the severity of the disease.
88 children of both sexes, between 1 and 4 years old, with a SCORAD of 25-50 will be selected as a part of routine outpatient visits at the Pediatric Allergy Department of the University Hospital of Verona.
The study product (active or placebo) will be administered for 3 months, with a follow-up period of further 3 months. From all participants, at time 0 and after 3 months, blood and stool samples will be collected for the analysis of vitamin D and cathelicidin levels and for the analysis of microflora respectively.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atopic Dermatitis
Keywords
atopic dermatitis, probiotics, vitamin D3, L. reuteri
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
88 (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 3 months
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Patients should take 10 drops once a day during meals for 3 months
Intervention Type
Dietary Supplement
Intervention Name(s)
Reuterin 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
SCORAD improvement
Description
Improvement of the SCORAD compared to baseline
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Vitamin D levels increase
Description
Increase of the levels of Vit. D compared to baseline
Time Frame
3 months
Title
LL-37 levels increase
Description
Increase of the levels of cathelicidin compared to baseline
Time Frame
3 months
Title
Changes in the fecal microflora
Description
Changes in the fecal microflora compared to baseline
Time Frame
3 months
Title
QoL improvement
Description
Improvement of the child's quality of life
Time Frame
3 months
Other Pre-specified Outcome Measures:
Title
Food Frequency Questionnaire
Description
Evaluation of the child's eating habits
Time Frame
3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
1 Year
Maximum Age & Unit of Time
4 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
diagnosis of atopic dermatitis of mild to moderate grade (SCORAD 25-50)
signature of the informed consent from both parents or a legal representative
Exclusion Criteria:
presence of autoimmune diseases, immunodeficiency, inflammatory bowel diseases, cystic fibrosis, metabolic diseases
use of immunosuppressive drugs and/or systemic corticosteroids in the previous 2 months
use of antibiotics in the last 4 weeks
use of probiotics and/or prebiotics in the last 2 weeks
use of vitamin D in the last 4 weeks
participation in other clinical trials
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Attilio Boner, Professor
Organizational Affiliation
Policlinico G.B. Rossi, Head of the Pediatric Department
Official's Role
Principal Investigator
Facility Information:
Facility Name
Policlinico G.B. Rossi
City
Verona
ZIP/Postal Code
37134
Country
Italy
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Effects of Lactobacillus Reuteri Plus Vitamin D3 in Children With Atopic Dermatitis
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