CClinicalTrials.gg
CompletedNCT05607511Updated Feb 8, 2024

GB-EZ-SIM03 Probiotics Study for Childhood Eczema

An interventional study of Probiotics baby immunity formula (SIM03) in Eczema, sponsored by Chinese University of Hong Kong. Completed at 1 site in Hong Kong. Open to participants aged 1 Year to 5 Years. Per ClinicalTrials.gov, last updated 2024-02-08.

Sponsored by Chinese University of Hong Kong · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 6 months after the study started (first participant enrolled Apr 2022, registered Oct 2022).
Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Not applicable
Ages
1 Year to 5 Years
Sex
All
01

Study 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.

Read the 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

  1. 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;
  2. 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.
02

Conditions studied

  • Eczema

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Keywords

  • Eczema
  • Probiotics
  • Open-label study
  • Microbiome
  • Children
03

In context

Eczema

1,084 studies on the registry are indexed under Eczema; 137 are open to participants now.

This study's enrollment of 20 is below the median of 80 across 861 interventional studies indexed under Eczema.

Browse Eczema studies →

Lead sponsor

Chinese University of Hong Kong is the lead sponsor of 1,419 studies on the registry; 487 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
1 Year to 5 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Children aged 1 to 5 years old with physician-diagnosed eczema according to Hanifin and Rakja criteria [22,23];
  2. 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

Exclusion Criteria:

  1. 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.
  2. 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.
  3. Children with eczema who require systemic immunosuppressive treatments (e.g. corticosteroid, azathioprine, biologics) within six months prior to recruitment.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
20 participants (actual)

Study arms

  • Experimental
    Active probiotics arm

    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.

    Other: Probiotics baby immunity formula (SIM03)

Interventions

  • OtherProbiotics baby immunity formula (SIM03)

    Daily oral intake of a probiotics sachet

06

What researchers measure

Primary outcomes

  1. Total score for SCORing Atopic Dermatitis (SCORAD)

    Combined endpoint

    Time frame: 3 months

  2. Stool frequency

    Combined endpoint

    Time frame: 3 months

  3. Stool consistency

    Combined endpoint

    Time frame: 3 months

Secondary outcomes

  1. Subjective SCORAD score

    Disease severity

    Time frame: 3 months

  2. Objective SCORAD score

    Disease severity

    Time frame: 3 months

  3. The change of stool frequency

    Stool condition

    Time frame: 3 months

  4. The change of stool consistency assessed using Bristol Stool Chart

    Stool condition

    Time frame: 3 months

  5. 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

    Time frame: 3 months

  6. Changes in faecal microbial profiling

    Gut microbiome

    Time frame: 3 months

  7. The biophysical condition of skin as measured by TransEpidermal Water Loss

    Skin biophysical parameters

    Time frame: 3 months

  8. The biophysical condition of skin as measured by Skin Hydration

    Skin biophysical parameters

    Time frame: 3 months

  9. Adverse events reported during the study period

    Monitoring of adverse events

    Time frame: 3 months

07

Study locations

1 site
  • Department of Paediatrics, Prince of Wales Hospital, 30-32 Ngan Shing Street, Shatin
    Hong Kong, 0000, Hong Kong
08

References and documents

Individual participant data

Plan to share: No — 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.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 8, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05607511
Lead sponsor
Chinese University of Hong Kong
Responsible party
Ting-fan Leung (Alice Ho Miu Ling Nethersole Charity Foundation Professor of Paediatrics, Chinese University of Hong Kong) — Principal investigator
First posted
Nov 7, 2022
Start date
Apr 1, 2022
Primary completion
Oct 31, 2022
Completion
Feb 5, 2024
Last update
Feb 8, 2024

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Feb 2024. You cannot join it, but the record below documents what was studied.

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