ClinicalTrials.gg
RecruitingNCT05794815Updated Aug 22, 2023

Modulation of Gut Microbiota by Probiotic in Children With Respiratory Symptoms

An interventional study of Probiotic and Placebo in Respiratory Infection (for Example, Pneumonia, Bronchitis), sponsored by Min-Tze LIONG. Recruiting at 1 site in Malaysia. Open to participants aged 12 Months to 7 Years. Per ClinicalTrials.gov, last updated 2023-08-22.

Sponsored by Min-Tze LIONG · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by May 2026, 6 months ago, but the record still lists the study as recruiting.
  • Started May 2023; still recruiting 3 years 6 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
120
Allocation
Randomized
Ages
12 Months to 7 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 14 studies testing probiotic in Respiratory Tract Infections — 3 open to participants now, 4 under way, none of them phase 3. Probiotic · Respiratory Tract Infections.

Planned enrollment
7th of 13
120 · median 120
Started
2023
with 2 others
No phase
11 of 14
2 open now
Registered
12th of 14
by date
Lead sponsor
3 of 14
Min-Tze LIONG

Among the 14 studies testing probiotic in Respiratory Tract Infections, this one is the 7th largest by planned enrollment of the 13 interventional ones, is one of 3 that started in 2023, is one of 11 with no phase, and was the 12th registered.

By phase

14 studies; the count open now beside each. This study's row is marked.

No phasethis study11 · 2 open
Phase 22 · 1 open
Phase 31 · 0 open

By the year they started

First in 2012; this study’s year is marked. 3 started in 2023.

Size and results

Median enrollment 120 across the 13 interventional studies. Of the 10 that completed or were terminated, 1 (10%) have results posted.

Watch this landscapeDownload CSVWith an account: a weekly mail of what changed among 14 studies testing probiotic in Respiratory Tract Infections, or all of them as a file.
02

Study summary

This project aims to study the benefits of probiotics namely Bifidobacterium infantis YLGB-1496 in modulating gut microbiota of children with respiratory symptoms, among pre-school children in Malaysia aged >12 months old, \<7 years old.

Read the detailed description

Probiotic can be defined as "live microorganisms that grant health effects to the host if consumed in sufficient amounts". Probiotic bacteria, which beneficially affect the host by improving the intestinal microbial balance, may affect the immune response, thus boosting the body system to combat against diseases.

Respiratory illnesses are the most common acute diseases in children where no virtually effective treatments or prophylaxes are available for these infections. Probiotics on the other hand have gained increasing evidences as an effective therapy in preventing respiratory tract infections. Children attending day care are especially at risk for acquiring respiratory illness, as close physical contact among children in day care favour the transmission of infectious diseases. When studying children receiving either probiotic in milk and control milk, the number of absences from day care because of illness is significantly lesser in probiotic group when compared with control group. In addition, children in the probiotic group had fewer respiratory tract infections with complications (otitis media, sinusitis, bronchitis and pneumonia) and less prescribed antibiotic treatments. The time without respiratory symptoms was also significantly longer in the probiotic group compared with the control group. When the effects of probiotics were studied on nasopharyngeal carriage of bacterial pathogens, the number of human bocavirus was reduced significantly in the nasopharynx of these children, indicating that probiotics may be more effective against respiratory tract infections of viral origin. While the precise mechanisms of using probiotics in management of respiratory infections are largely unknown, speculations include: probiotics compete against pathogens; increase the barrier function in respiratory epithelium; immunostimulatory effects by enhancing cellular immunity with increased activity of natural killer cells and macrophages in airways. Hence, probiotics may offer safe means of reducing the risk of early respiratory related illnesses, common cold and antibiotic use, and the risk of recurrent respiratory infections, thereby represent a simple, safe, effective, available and affordable method for preventing respiratory infections in children.

In worldwide, it is estimated that 5.2 million of children under five of age die every year due to preventable disease such as diarrhea, malaria and pneumonia. Up to date, diarrhea still remains as global health issues, even in developing countries, with 1 million of children deaths reported to be attributed to diarrhea. In Malaysia, reported cases of diarrhea and acute gastroenteritis have been observed to occur throughout the year, with rotavirus-associated diarrhea being the most prevalently identified gastrointestinal disorder. One of the most common gastrointestinal disorders in young children, is diarrhea. Diarrhea is commonly defined as three or more loose or watery stools in the last 24 hours. For clinical studies employing oral administration of probiotics, the probiotics were administered directly to the participants or mixed with a variety of fluids and foods. In studies on probiotic prevention of acute diarrhea in daycare centres worldwide, probiotics tested such as Lactobacillus GG, Bifidobacterium lactis (alone or in combination with Streptococcus thermophiles), and Lactobacillus reuteri, Lactobacillus casei and Lactobacillus acidophilus showed a clear evidence of efficacy to reduce diarrhea-related symptoms in a strain-dependent and dose-dependent manner. Probiotics administration reduces duration of diarrhea, indicating the efficacy of probiotics not only in preventing occurrence of diarrhea, as well as to treat episodes of diarrhea. Probiotics Lactobacillus acidophilus, Lactobacillus rhamnosus, Bifidobacterium longum and Saccharomyces boulardii also showed decreased time of vomiting in the intervention groups as compared with controls during the probiotics treatment of acute rotavirus diarrhoea. The rationale for using probiotics in infectious diarrhoea is that they act against enteric pathogens by competing for available nutrients and binding sites, making the gut contents acid, producing a variety of chemicals, and increasing specific and non-specific immune responses. Probiotics reduced infectious diarrhoea in children and adults in various settings but a mechanism common to most probiotics, for example, colonization resistance, is effective against a wide range of gut pathogens.

Probiotic bacteria, which beneficially affect the host by improving the intestinal microbial balance, may affect the immune response, thus boosting the body system to combat against diseases. Probiotics have been studied extensively for their effects in preventing and treating a multitude of conditions, including the treatment of lactose intolerance, traveller's diarrhoea and the prevention and treatment of nosocomial diarrhoea. In acute diarrhoea, a reduction in the frequency of diarrhoeal symptoms has been reported in adults and children treated with probiotics. Among the beneficial microbes, Bifidobacterium is one of the best-known probiotic genus in the world, and it is widely applied in the dairy industry as a probiotic. Evidences from in vitro, in vivo, and clinical studies and long consumption history support the safety and health benefits of Bifidobacterium strains. The ingestion of yogurt fortified with B. longum reduced harmful bacteria such as Enterobacteriaceae, Streptococcus and C. perfringens, while at the same time alter the microbiota gut profile of volunteers with a significant increase of beneficial microbes Bifidobacterium and Lactobacillus species. Additionally, putrefactive substances in the intestinal environment were also reduced in the presence of the probiotic supplement. Such findings suggest that Bifidobacterium strains are safe and could be used further to evaluate its effect in preventing diarrhea and/or respiratory-related illness prevalence in young children.

Probiotic (Bifidobacterium infantis YLGB-1496) adheres to probiotic properties such as excellent tolerance to gastric acid, intestinal fluid and bile salt of the digestive system. Both probiotic and placebo products are manufactured under HACCP conditions. All products do not contain any animal-origin ingredients. The probiotic product contains probiotic and carrier while placebo contains only carrier. Sachets of products containing probiotic and placebo appear as light yellow powder. Both probiotic and placebo products are kept at storage temperature range below 30oC according to the condition recommended by the manufacturer.

03

Conditions studied

  • Respiratory Infection (for Example, Pneumonia, Bronchitis)

Keywords

  • probiotic
  • respiratory tract infections
  • Bifidobacterium
  • children
04

Who can participate

Ages eligible
12 Months to 7 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Preschool children (>12 months old, \<7 years old).
  • Having respiratory symptoms (having at least two of the following signs and symptoms: fever (even if only reported not measured), nasal obstruction, chills, sore throat, headache, cough, runny nose, olfactory disturbances, or taste disturbances; Pucarelli-Lebreiro et al., 2022).
  • Healthy with current weight of P20-P80 percentile chart of children
  • Infant formula powder does not contain probiotics; prebiotics FOS is not allowed, GOS \<2g/ 100g is allowed
  • Willing to commit throughout the experiment

Exclusion criteria

Exclusion Criteria:

  • Long term medication >6 months for any diseases
  • Deformity
  • Mothers with metabolic and/or chronic diseases
  • Current or previous diseases, conditions or interventions that may interfere with the study (such as tolerance and/or growth and development), such as gastrointestinal malformations, chronic diarrhea, malabsorption syndromes, malnutrition, congenital immunodeficiency or surgery
  • Oral antibiotics within 2 weeks before the intervention
  • Nutritional supplements containing probiotics and prebiotics (except infant formula) within 2 weeks before the intervention
  • Foods for special medical purposes or non-standard formula powders for lactose intolerance and galactosemia
  • Probiotic allergies or possible food allergies (milk, etc.)
  • Participated in other clinical studies 4 weeks before the intervention
  • Unwilling to participate for any particular reason
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Care provider, Investigator)
Enrollment
120 participants (estimated)

Study arms

  • Experimental
    Probiotic

    Bifidobacterium infantis YLGB-1496 at 1x10 log CFU/day for 12 weeks

    Dietary Supplement: Probiotic

  • Placebo comparator
    Placebo

    Intervention consists of daily administration of 2g of maltodextrin, administered daily for 12-weeks)

    Dietary Supplement: Placebo

Interventions

  • Dietary supplementProbiotic

    Bifidobacterium infantis YLGB-1496 at 1x10 log CFU/day for 12 weeks

  • Dietary supplementPlacebo

    Intervention consists of daily administration of 2g of maltodextrin, administered daily for 12-weeks)

06

What researchers measure

Primary outcomes

  1. Microbiota profiles of fecal samples in children with respiratory tract infections upon administration of probiotic as assessed via pyrosequencing

    Differences in microbiota abundance in fecal sample of children with respiratory tract infections upon administration o probiotic compared to placebo

    Time frame: 12-weeks

Secondary outcomes

  1. Clinical respiratory symptoms duration and frequency in children with respiratory tract infections upon administration of probiotic as assessed using the Monthly Health Questionnaire (as used in ClinicalTrials.gov (identifier number NCT02434042)

    Changes in duration and frequency of respiratory illnesses symptoms from children on probiotic or placebo after 12-weeks, via the use of questionnaire.

    Time frame: 12-weeks

  2. Clinical gastrointestinal symptoms in children with respiratory tract infections upon administration of probiotic as assessed using the Monthly Gastrointestinal Questionnaire as used in ClinicalTrials.gov (identifier number NCT02434042)

    Differences in duration and frequency of gastrointestinal symptoms of children upon administration of probiotic compared to placebo

    Time frame: 12-weeks

  3. Immunity profiles in children with respiratory tract infections upon administration of probiotic via the use of oral swabs

    Differences in concentrations of proteins such as interleukins (IL-10, IL-4, IL-6, Tumour Necrosis Factor-alpha, Interferon gamma) in swab samples (ug/mL) of children upon administration of probiotic compared to placebo

    Time frame: 12-weeks

07

Study locations

1 of 1 sites recruiting
  • UKM Medical Centre
    Cheras, Kuala Lumpur 56000, Malaysia
    Recruiting
    • Adli Adli, MD · Contactadli.ali@ppukm.ukm.edu.my · 603 8921 5555
    • Fahisham Taib, MD · Sub investigator
    • Intan Juliana Abd. Hamid, MD · Sub investigator
    • Min Tze Liong, PhD · Sub investigator
08

References and documents

Individual participant data

Plan to share: No

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 Aug 22, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05794815
Lead sponsor
Min-Tze LIONG
Responsible party
Min-Tze LIONG (Professor, Universiti Sains Malaysia) — Sponsor-investigator
First posted
Apr 3, 2023
Start date
May 1, 2023
Primary completion
May 1, 2026 (estimated)
Completion
May 1, 2026 (estimated)
Last update
Aug 22, 2023

Study contacts

Adli Ali, MD
Contact
adli.ali@ppukm.ukm.edu.my
603 8921 5555
Min Tze Liong, PhD
Contact
mintze.liong@usm.my
6046532114
Adli Ali, MD
principal investigator · National University of Malaysia

Oversight

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

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Studies of the drug tested here: Probiotic

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