Management of Eczema by Specific Probiotic Strains (BAMBOO)
Primary Purpose
Eczema, Atopic Dermatitis
Status
Withdrawn
Phase
Phase 3
Locations
Netherlands
Study Type
Interventional
Intervention
Ecologic ® Panda II
placebo
Sponsored by
About this trial
This is an interventional treatment trial for Eczema focused on measuring infants, adaptive immunology, atopic dermatitis, probiotics
Eligibility Criteria
Inclusion Criteria:
- children 0-15 months with mild to moderate eczema (SCORAD score 15-50 or equally EASI score) for at least two weeks
Exclusion Criteria:
- use of topical steroids class II or higher (which means treatment for severe eczema),
- use of oral steroids or treatment with antibiotics prior to inclusion.
- severe comorbidity
- lack of knowledge of the Dutch language
Sites / Locations
- St. Antonius Ziekenhuis
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
Probiotic mixture
Placebo mixture
Arm Description
participants daily ingest a selected probiotic mixture for a period of 3 months
controls daily ingest a placebo mixture for a period of 3 months.
Outcomes
Primary Outcome Measures
decrease in severity of atopic dermatitis
The primary outcome will be measured by change in the severity of AD by using the SCORAD score.
Other outcomes: subjective (parental) change in eczema severity, change in amount of and type of topical steroid use, quality of life during and after intervention (measured by ITQOL questionnaire), amount of respiratory tract infections, use of antibiotics, use of primary care medicine (general practitioner).
All used probiotic strains contain the QPS status. (serious) adverse events will be recorded systematically.
Secondary Outcome Measures
Effects on infant gut microbiota
Analyses will be done by molecular microbiological techniques on feces samples (that will be collected at baseline, and after 1,3 and 6 months after enrollment.
Effects on the immature immune system
These effects will be measured by analyzing serum IgE and different (Th1/Th2) cytokines and chemokines
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01230190
Brief Title
Management of Eczema by Specific Probiotic Strains
Acronym
BAMBOO
Official Title
Beyond Conventional Treatment of Atopic Eczema in Infants: Management By Specific prObiOtic Strains
Study Type
Interventional
2. Study Status
Record Verification Date
March 2011
Overall Recruitment Status
Withdrawn
Why Stopped
Because of safety issues/support concerning the multispecies probiotic mixture
Study Start Date
March 2011 (undefined)
Primary Completion Date
July 2011 (Anticipated)
Study Completion Date
July 2011 (Anticipated)
3. Sponsor/Collaborators
Name of the Sponsor
Agentschap NL
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
To investigate the therapeutic effect of a selected probiotic mixture on the severity of AD in infants aged 0-15 months. The probiotic mixture has been studied in laboratory setting and has proven IL-10 stimulating effects. Therefore it is thought to decrease AD severity in young children (beyond the conventional treatment).
Detailed Description
Atopic dermatitis (AD) is a highly prevalent chronic, itching, inflammatory skin disease that often presents in infancy. The disease can be the first manifestation of the so-called atopic march, the natural progression of allergic disorders, with subsequent development of asthma and allergic rhinitis. Approximately 40% of the children with AD will develop asthma later in childhood.
Currently, topical corticosteroids are the mainstay treatment of atopic dermatitis; however, relapses are common and parents often fear possible side-effects, leading to non-compliance. There is increasing evidence that the intestinal microbiota plays an important role in the development of allergic diseases. Modulation of the intestinal microbiota with probiotics, living micro-organisms with immunomodulatory effects, could possibly offer a new way of treatment of allergic disease.
Clinical trials investigating the preventive as well as therapeutic effect of probiotics on atopic dermatitis show inconsistent results. Systematic (Cochrane) reviews of all clinical trials (about treatment of AD by use of probiotics) concluded that the probiotic strains studied to date are not an effective treatment for AD; however, there is great heterogeneity between studies since many different probiotic strains are used. Because of the known strain specific capacity in immunomodulatory effects, some strains might have a greater effect than others.
Better results can possibly be achieved by using a selected, (in laboratory setting) proven modulatory multispecies probiotic mixture, containing 6 different strains.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Eczema, Atopic Dermatitis
Keywords
infants, adaptive immunology, atopic dermatitis, probiotics
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Probiotic mixture
Arm Type
Active Comparator
Arm Description
participants daily ingest a selected probiotic mixture for a period of 3 months
Arm Title
Placebo mixture
Arm Type
Placebo Comparator
Arm Description
controls daily ingest a placebo mixture for a period of 3 months.
Intervention Type
Dietary Supplement
Intervention Name(s)
Ecologic ® Panda II
Other Intervention Name(s)
multispecies probiotic mixture
Intervention Description
Probiotic strains: 3 Bifidobacteria, 3 Lactococci, 1*10^9 Colony Forming Units/g.
Composition: rice starch, maltodextrins, bacterial strains and mix of minerals.
Intervention Type
Dietary Supplement
Intervention Name(s)
placebo
Other Intervention Name(s)
placebo mixture
Intervention Description
rice starch, maltodextrins, and mix of minerals. The placebo mixture is similar in aspect, consistency and taste as Ecologic ® Panda II (intervention).
Primary Outcome Measure Information:
Title
decrease in severity of atopic dermatitis
Description
The primary outcome will be measured by change in the severity of AD by using the SCORAD score.
Other outcomes: subjective (parental) change in eczema severity, change in amount of and type of topical steroid use, quality of life during and after intervention (measured by ITQOL questionnaire), amount of respiratory tract infections, use of antibiotics, use of primary care medicine (general practitioner).
All used probiotic strains contain the QPS status. (serious) adverse events will be recorded systematically.
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Effects on infant gut microbiota
Description
Analyses will be done by molecular microbiological techniques on feces samples (that will be collected at baseline, and after 1,3 and 6 months after enrollment.
Time Frame
6 months
Title
Effects on the immature immune system
Description
These effects will be measured by analyzing serum IgE and different (Th1/Th2) cytokines and chemokines
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
1 Day
Maximum Age & Unit of Time
15 Months
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
children 0-15 months with mild to moderate eczema (SCORAD score 15-50 or equally EASI score) for at least two weeks
Exclusion Criteria:
use of topical steroids class II or higher (which means treatment for severe eczema),
use of oral steroids or treatment with antibiotics prior to inclusion.
severe comorbidity
lack of knowledge of the Dutch language
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Arine M Vlieger, MD, PhD
Organizational Affiliation
St. Antonius Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
St. Antonius Ziekenhuis
City
Nieuwegein
State/Province
Utrecht
ZIP/Postal Code
3430 EM
Country
Netherlands
12. IPD Sharing Statement
Learn more about this trial
Management of Eczema by Specific Probiotic Strains
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