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.
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
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.
- Conditions
- Overweight , 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 group | Role | What they receive |
|---|---|---|
| Probiotic | Experimental | One 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 |
| Placebo | Placebo comparator | A 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.
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)
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
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
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
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.
- First posted4 Mar 2026
- Study start1 Dec 2023
- Primary completion1 Apr 2026 (estimated)
- Study completion1 Apr 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Overweight , ObesityStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Min-Tze LIONG
- Sponsor type
- University, hospital or other
- Collaborators
- Nanxiang Hospital Shanghai
- Responsible party
- Sponsor-investigator, Min-Tze LIONG, Universiti Sains Malaysia
- Investigators
- Aihua Zhang, MD., Principal investigator, Nanxiang Hospital, Jiading District, Shanghai
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
Study at a glance
From the registry record, last updated by the sponsor on 4 Mar 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Study on the Efficacy of Probiotics in the Treatment of Childhood Obesity and Their Effects on Gut Microbiota
- ClinicalTrials.gov ID
- NCT07448220
- Acronym / sponsor ID
- 2023-1116-10
- Conditions
- Overweight , Obesity
- Keywords
- overweight, obesity, Bifidobacterium, children
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Active, not recruiting
- Enrolment
- 60 participants (estimated)
- Lead sponsor
- Min-Tze LIONGUniversity, hospital or other
- Collaborators
- Nanxiang Hospital Shanghai
- Study start
- 1 Dec 2023 (actual)
- Primary completion
- 1 Apr 2026 (estimated)
- Study completion
- 1 Apr 2026 (estimated)
- First posted
- 4 Mar 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind (participant, care provider, investigator)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Probiotic | Experimental | Dietary Supplement: ProbioticOne sachet containing Bifidobacterium longum subsp. longum dipro O + Bifidobacterium longum subsp. longum dipro X, at a dose of 5 × 10^9 CFU per day. |
| Placebo | Placebo comparator | Dietary Supplement: PlaceboA sachet of maltodextrin per day. |
Who may qualify
- Ages
- 3 to 14 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child
Key inclusion criteria (3 listed)
- 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.
Key exclusion criteria (5 listed)
- 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.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| ProbioticA sachet of Bifidobacterium longum subsp. longum dipro O + Bifidobacterium longum subsp. longum dipro X, at a dose of 5 × 10^9 CFU per day. | Dietary supplement | Probiotic |
| PlaceboA sachet of maltodextrin per day. | Dietary supplement | Placebo |
Primary outcome
Body Mass Index (BMI) percentile in children upon administration of probiotics or placebo as assessed anthropometrically
Time frame: 8 weeks
Differences in BMI percentile in children upon administration of probiotics or placebo
4 secondary outcomes
Height (cm) of children upon administration of probiotics or placebo as assessed anthropometrically
Time frame: 8 weeks
Microbiota profiles of fecal samples in children upon administration of probiotics or placebo as assessed via 16s rRNA gene sequencing
Time frame: 8 weeks
Weight (kg) of children upon administration of probiotics or placebo as assessed anthropometrically
Time frame: 8 weeks
Waist circumference (cm) of children upon administration of probiotics or placebo as assessed anthropometrically
Time frame: 8 weeks
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 4 Mar 2026.
- Individual participant dataSharing planned: No
Related trials for Overweight , Obesity
RecruitingObservational study
Endoscopic Sleeve Gastroplasty (ESG) Prospective Trial for Obesity (EGO-Trial)
Obesity
Active, not recruitingPhase 4
Effects of Sequential Therapy With Mexidol® (Intravenous) and Mexidol® FORTE 250 (Oral) on Functional Brain Activity Assessed by Functional Magnetic Resonance Imaging and Biochemical Parameters in Patients With Chronic Cerebral Ischemia: A Comparison of Patients With and Without Metabolic Disorders
Metabolic Abnormalities, Obesity & Overweight
Recruiting
Exercise Training and Vitamin D Metabolism
Obesity & Overweight, Vitamin D
Recruiting
Metabolic Health, Bones and Nuts During Weight Loss in Adults
Weight Loss, Bone Density
Active, not recruiting
Effect of Probiotics on Insulin Sensitivity in Overweight and Obese Pregnancy
Obesity & Overweight, Gestational Diabetes Mellitus (GDM)
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Aihua Zhang, MD. principal investigator
Nanxiang Hospital, Jiading District, Shanghai
2 sites in 2 countries: see every site and its status.
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.