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GB-EZ-SIM03 Probiotics Study for Childhood Eczema

Primary Purpose

Eczema

Status
Active
Phase
Not Applicable
Locations
Hong Kong
Study Type
Interventional
Intervention
Probiotics baby immunity formula (SIM03)
Sponsored by
Chinese University of Hong Kong
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Eczema focused on measuring Eczema, Probiotics, Open-label study, Microbiome, Children

Eligibility Criteria

1 Year - 5 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Children aged 1 to 5 years old with physician-diagnosed eczema according to Hanifin and Rakja criteria [22,23]; One of the parents or legal guardian (no mental illness or dementia, etc. that will hinder their ability to undertake informed consent) will provide written informed consent. Exclusion Criteria: Children with other documented chronic and clinically significant dermatologic diseases, such as erythra, that may interfere with evaluation of cutaneous microbiome. Common transient conditions such as acne are permissible. Children with eczema who have taken antibiotics, probiotics or prebiotics in supplement, including but not limited to growing-up milk formula and infant's supplementary food within three months prior to inclusion. Children with eczema who require systemic immunosuppressive treatments (e.g. corticosteroid, azathioprine, biologics) within six months prior to recruitment.

Sites / Locations

  • Department of Paediatrics, Prince of Wales Hospital, 30-32 Ngan Shing Street, Shatin

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Active probiotics arm

Arm Description

The SIM03 (supplied by GenieBiome Limited and produced under Good Manufacturing Practice, GMP) contains a blend of naturally occurring food-grade Bifidobacterium strains (1 billion CFU in 1 sachet). Recruited subjects will receive one sachet of baby immunity formula SIM03 twice daily for 3 months.

Outcomes

Primary Outcome Measures

Total score for SCORing Atopic Dermatitis (SCORAD)
Combined endpoint
Stool frequency
Combined endpoint
Stool consistency
Combined endpoint

Secondary Outcome Measures

Subjective SCORAD score
Disease severity
Objective SCORAD score
Disease severity
The change of stool frequency
Stool condition
The change of stool consistency assessed using Bristol Stool Chart
Stool condition
Quality of life assessment using a skin-specific Children's Dermatology Life Quality Index (CDLQI) and Infants' Dermatitis Quality of Life Index (IDQOL)
Quality of life related to eczema
Changes in faecal microbial profiling
Gut microbiome
The biophysical condition of skin as measured by TransEpidermal Water Loss
Skin biophysical parameters
The biophysical condition of skin as measured by Skin Hydration
Skin biophysical parameters
Adverse events reported during the study period
Monitoring of adverse events

Full Information

First Posted
October 28, 2022
Last Updated
September 1, 2023
Sponsor
Chinese University of Hong Kong
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1. Study Identification

Unique Protocol Identification Number
NCT05607511
Brief Title
GB-EZ-SIM03 Probiotics Study for Childhood Eczema
Official Title
Improvement in Eczema and the Safety of Microbiome Baby Immunity Formula (SIM03) on Childhood Eczema Development - A Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
April 1, 2022 (Actual)
Primary Completion Date
October 31, 2022 (Actual)
Study Completion Date
April 30, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chinese University of Hong Kong

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
Eczema is the most prevalent chronic skin disease in young children, and skin infection is commonly seen during eczema flare. Dysbiosis is increasingly recognised in the stool and skin of these patients. It is a common practice for parents to start these eczematous children on probiotics, but there is limited evidence if this treatment works in young patients. This single-centre, open-label clinical trial aims to investigate the benefits of a 3-month treatment of young children with eczema with a new probiotics called microbiome baby immunity formula (SIM03). Study outcomes include eczema severity, quality of life, biophysical measures of the skin and gastrointestinal symptoms, while adverse events related to this probiotics treatment will be monitored. The effects of this intervention on stool microbiome will also be analysed.
Detailed Description
Eczema is a common chronic skin disease that affects a substantial part of population. The associated economic burden was estimated to cost more than $5 billion per year with the rising prevalence of this disease worldwide. A 2016 nation-wide study in China reported that 12.9% of children (1-7 years) were diagnosed with eczema. Growing evidence has shown that atopic dermatitis and/or eczema would increase the risk of several diseases' development, including stroke, myocardial infarction, unstable angina, atrial fibrillation, and cardiovascular death. Except variation of clinical symptoms including dryness and itchy skin in eczema patients, gastrointestinal symptoms were also reported by children with atopic eczema, such as abdominal pain, abdominal distension, diarrhoea, constipation, vomiting and regurgitation. Unique gastrointestinal microflora pattern has also been observed in atopic dermatitis/ eczema patients when compared with healthy controls: decreased Bifidobacterium and Enterococci, especially Bifidobacterium bifidum and Bifidobacterium longum, and increased Faecalibacterium have been observed. Therefore, gastrointestinal microflora can serve as the disease indicator of eczema. The development of gut microbiota starts before birth. The infant's microbiome can impact on human health in later life. To prevent disease, we need to nip it in the bud. Emerging evidence suggests that gut microbiota modulation can largely affect host immune functions in children and adults. To date, no baby formula is specific for alleviating eczema-related symptoms for small children. GenieBiome Limited, a microbiome research-based company in Hong Kong developed a unique oral microbiome formula (baby immunity formula, SIM03) to prevent or treat gut dysbiosis and eczema development. SIM03 contains a blend of naturally occurring two food-grade probiotics strains, two prebiotics and two postbiotics. The two probiotics belong to food-grade Bifidobacterium, which is an important group of probiotic cultures commonly used in food products. Especially, research showed that Bifidobacterium could displace the proteolytic bacteria causing diarrhoea and recommended the administration of bifidobacteria to infants suffering from this symptom. Whereas the two prebiotics belong to food-grade oligosaccharides, which have been already used in food products. The two postbiotics belong to the acetates, which are also food grade and allowed to add in the foods. We hypothesize that the gut microbiota of children with eczema can be modulated to decrease the severity of eczema related symptoms and the condition can be improved. A pilot study is proposed to assess the effect and safety of SIM03 on eczema severity, gut microbiome and GI symptoms of the children with eczema. HYPOTHESIS We hypothesize that the microbiome baby immunity formula (SIM03) will lead to the improvement of eczema symptoms in children 1-5 years of age. OBJECTIVES To examine the effects of SIM03 in modulating gut microbiota, and improving the eczema severity, stool frequency/consistency in children aged 1-5 years old who have eczema; To evaluate the safety of SIM03 by assessing the parent-reported adverse events in children aged 1-5 years old who have eczema in 1-5 years old children.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Eczema
Keywords
Eczema, Probiotics, Open-label study, Microbiome, Children

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Single-group, open-label interventional clinical trial
Masking
None (Open Label)
Masking Description
Masked laboratory staff about the clinical details and disease-related information of participants.
Allocation
N/A
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Active probiotics arm
Arm Type
Experimental
Arm Description
The SIM03 (supplied by GenieBiome Limited and produced under Good Manufacturing Practice, GMP) contains a blend of naturally occurring food-grade Bifidobacterium strains (1 billion CFU in 1 sachet). Recruited subjects will receive one sachet of baby immunity formula SIM03 twice daily for 3 months.
Intervention Type
Other
Intervention Name(s)
Probiotics baby immunity formula (SIM03)
Intervention Description
Daily oral intake of a probiotics sachet
Primary Outcome Measure Information:
Title
Total score for SCORing Atopic Dermatitis (SCORAD)
Description
Combined endpoint
Time Frame
3 months
Title
Stool frequency
Description
Combined endpoint
Time Frame
3 months
Title
Stool consistency
Description
Combined endpoint
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Subjective SCORAD score
Description
Disease severity
Time Frame
3 months
Title
Objective SCORAD score
Description
Disease severity
Time Frame
3 months
Title
The change of stool frequency
Description
Stool condition
Time Frame
3 months
Title
The change of stool consistency assessed using Bristol Stool Chart
Description
Stool condition
Time Frame
3 months
Title
Quality of life assessment using a skin-specific Children's Dermatology Life Quality Index (CDLQI) and Infants' Dermatitis Quality of Life Index (IDQOL)
Description
Quality of life related to eczema
Time Frame
3 months
Title
Changes in faecal microbial profiling
Description
Gut microbiome
Time Frame
3 months
Title
The biophysical condition of skin as measured by TransEpidermal Water Loss
Description
Skin biophysical parameters
Time Frame
3 months
Title
The biophysical condition of skin as measured by Skin Hydration
Description
Skin biophysical parameters
Time Frame
3 months
Title
Adverse events reported during the study period
Description
Monitoring of adverse events
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Year
Maximum Age & Unit of Time
5 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Children aged 1 to 5 years old with physician-diagnosed eczema according to Hanifin and Rakja criteria [22,23]; One of the parents or legal guardian (no mental illness or dementia, etc. that will hinder their ability to undertake informed consent) will provide written informed consent. Exclusion Criteria: Children with other documented chronic and clinically significant dermatologic diseases, such as erythra, that may interfere with evaluation of cutaneous microbiome. Common transient conditions such as acne are permissible. Children with eczema who have taken antibiotics, probiotics or prebiotics in supplement, including but not limited to growing-up milk formula and infant's supplementary food within three months prior to inclusion. Children with eczema who require systemic immunosuppressive treatments (e.g. corticosteroid, azathioprine, biologics) within six months prior to recruitment.
Facility Information:
Facility Name
Department of Paediatrics, Prince of Wales Hospital, 30-32 Ngan Shing Street, Shatin
City
Hong Kong
ZIP/Postal Code
0000
Country
Hong Kong

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
No need to disclose individual study data in this simple open-label clinical trial, thus it will report only the aggregate and summary of study findings from participants.

Learn more about this trial

GB-EZ-SIM03 Probiotics Study for Childhood Eczema

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