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Overweight , ObesityPhase 2NCT07448220

Study on the Efficacy of Probiotics in the Treatment of Childhood Obesity and Their Effects on Gut Microbiota

A Phase 2 study testing Probiotic in people with Overweight , Obesity, run by Min-Tze LIONG at 2 sites in 2 countries.

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record
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Trial summary

This interventional study aims to evaluate the efficacy of a probiotics supplementation (Bifidobacterium longum subsp. longum Dipro-O and Bifidobacterium longum subsp. longum Dipro-X; dipro Gracfor PROBIOTICS FAST MELT) in treating childhood obesity and its impact on gut microbiota. Read more about this study

Who is it for?
Ages 3 to 14 yearsHealthy volunteers can take part
Conditions the study is for
Overweight , Obesity
What is being tested?
Probiotic
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
60 participants
Where
2 sitesin 2 countries
Study dates
1 Dec 2023to 1 Apr 2026
Phase
Phase 2
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 3 to 14 years
  • All sexes
  • Healthy volunteers accepted
  • Child

Who may be able to join

  • Diagnostic Criteria (Refer to the "Expert Consensus on Diagnosis and Management of Childhood Obesity in China"): For children aged 2-5 years, refer to the "Growth Curve for Chinese Children and Adolescents Aged 0-18 Years" to determine the BMI cutoff points for overweight and obesity in Chinese children aged 2-5 years. For children aged 6-18 years, refer to the "Screening for Overweight and Obesity in School-Age Children and Adolescents" to determine the BMI cutoff points for overweight and obesity by age and gender in children aged 6-18 years.
  • Age: 3-14 years.
  • Fully informed consent: Parents or guardians have been fully informed of the clinical trial procedures, and both have signed the written informed consent form.

Who cannot join

  • The child has chronic or severe systemic diseases.
  • The child has a family history of obesity-related metabolic or endocrine diseases.
  • The child has been diagnosed with psychological disorders or psychiatric diseases.
  • The child has used antibiotics or probiotic preparations within 4 weeks prior to enrollment.
  • The child was enrolled in other clinical studies 4 weeks prior to enrollment.

Trial locations and contacts

2 sites in 2 countries.

2 sites in 2 countries

China1 site
  • Nanxiang Hospital, Jiading District, Shanghai

    Jiading, Shanghai Municipality, 201800

Other trials in China

Malaysia1 site
  • Universiti Sains Malaysia

    Pulau Pinang, Pulau Pinang, 11800

Other trials in Malaysia

About this study

This interventional study aims to evaluate the efficacy of a probiotics supplementation (Bifidobacterium longum subsp. longum Dipro-O and Bifidobacterium longum subsp. longum Dipro-X; dipro Gracfor PROBIOTICS FAST MELT) in treating childhood obesity and its impact on gut microbiota. The study will enroll 60 overweight or obese children aged 3 to 14 years. Participants will be randomly assigned to either a treatment group receiving lifestyle intervention combined with an oral Bifidobacterium preparations for 8 weeks, or a control group receiving lifestyle intervention alone. The primary outcome is the change in sex-specific BMI-for-age percentiles. Secondary outcomes include changes in height, weight, waist circumference, quality of life satisfaction, and alterations in gut microbiota composition analyzed via 16S rRNA gene sequencing.

Read the detailed description

Childhood obesity has emerged as one of the most serious public health challenges of the 21st century, with prevalence rates increasing dramatically worldwide. In China, the combined prevalence of overweight and obesity among children and adolescents has risen sharply over the past two decades, affecting approximately one in five school-aged children. This condition is associated with a range of adverse health outcomes, including metabolic disturbances, cardiovascular risk factors, and psychosocial complications, many of which can track into adulthood. Early intervention is widely recognized as critical for improving long-term health outcomes, underscoring the need for effective and sustainable therapeutic strategies. Growing evidence indicates that intestinal microbiota dysbiosis plays a key role in the pathogenesis of obesity. Studies have consistently reported alterations in the gut microbial composition of obese individuals compared to normal-weight controls, characterized by reduced microbial diversity and changes in the relative abundances of specific bacterial phyla. Specifically, a decreased proportion of beneficial bacteria such as Bifidobacterium and an increased ratio of Firmicutes to Bacteroidetes have been frequently observed in obese populations. These findings have spurred interest in microbiota-targeted interventions, particularly the use of probiotics, for weight management. Among probiotic strains, Bifidobacterium species have attracted considerable attention due to their potential to modulate host energy metabolism, reduce adiposity, and improve metabolic parameters. Preclinical studies in murine models have demonstrated that Bifidobacterium supplementation can attenuate diet-induced obesity by enhancing gut barrier function, reducing systemic inflammation, and regulating appetite-related hormones. However, despite promising preclinical evidence, clinical data in pediatric populations remain relatively limited, and the optimal strains, dosages, and treatment durations have yet to be definitively established. To address this gap, the present study is designed as a randomized, parallel-group, controlled clinical trial. It aims to evaluate the efficacy of a Bifidobacterium probiotics combination in overweight and obese children aged 3 to 14 years. The study specifically assesses the intervention's effects on anthropometric parameters, including body mass index (BMI) percentile and height, weight and waist circumference, and explores correlations between gut microbiota changes and clinical improvements. Participants will be randomly assigned to receive either lifestyle intervention combined with oral Bifidobacterium probiotics or lifestyle intervention alone for a duration of 8 weeks. The primary outcome is the change in BMI percentile from baseline to the end of the intervention period. Secondary outcomes include changes in height, weight, waist circumference, parental-reported quality of life satisfaction, and alterations in gut microbiota composition as assessed by 16S rRNA gene sequencing of fecal samples. By investigating both the clinical efficacy and the underlying microbiological mechanisms, this study is intended to support the development of evidence-based, targeted microbial interventions for childhood obesity.

Being tested
Probiotic, Placebo
Keywords
overweight, obesity, Bifidobacterium, children
Medical subject headings
Overweight, Obesity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • ProbioticDietary supplement

    A sachet of Bifidobacterium longum subsp. longum dipro O + Bifidobacterium longum subsp. longum dipro X, at a dose of 5 × 10^9 CFU per day.

  • PlaceboDietary supplement

    A sachet of maltodextrin per day.

Study groups in NCT07448220
Study groupRoleWhat they receive
ProbioticExperimentalOne sachet containing Bifidobacterium longum subsp. longum dipro O + Bifidobacterium longum subsp. longum dipro X, at a dose of 5 × 10^9 CFU per day.
Receives: Dietary Supplement: Probiotic
PlaceboPlacebo comparatorA sachet of maltodextrin per day.
Receives: Dietary Supplement: Placebo

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Body Mass Index (BMI) percentile in children upon administration of probiotics or placebo as assessed anthropometrically

    Differences in BMI percentile in children upon administration of probiotics or placebo

    Measured: 8 weeks

Secondary outcomes (4)
  1. Height (cm) of children upon administration of probiotics or placebo as assessed anthropometrically

    Changes in height of children upon administration of probiotics or placebo

    Measured: 8 weeks

  2. Microbiota profiles of fecal samples in children upon administration of probiotics or placebo as assessed via 16s rRNA gene sequencing

    Differences in microbiota profiles in fecal sample of children upon administration probiotics or placebo

    Measured: 8 weeks

  3. Weight (kg) of children upon administration of probiotics or placebo as assessed anthropometrically

    Weight of children upon administration of probiotics or placebo

    Measured: 8 weeks

  4. Waist circumference (cm) of children upon administration of probiotics or placebo as assessed anthropometrically

    Waist circumference (cm) of children upon administration of probiotics or placebo

    Measured: 8 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted4 Mar 2026
  2. Study start1 Dec 2023
  3. Primary completion1 Apr 2026 (estimated)
  4. Study completion1 Apr 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Triple blind
Who is masked
Participant, Care provider, Investigator
Enrolment
60 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07448220
Sponsor's protocol ID
2023-1116-10
Status last verified
Feb 2026
First submitted
23 Feb 2026
Last updated
4 Mar 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing Probiotic in people with Overweight , Obesity, run by Min-Tze LIONG at 2 sites in 2 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: under way, not looking for participants, as of the sponsor's last update on 4 Mar 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in China, Malaysia. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Body Mass Index (BMI) percentile in children upon administration of probiotics or placebo as assessed anthropometrically (time frame: 8 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Mar 2026.

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