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Probiotics Effect on Glucose and Lipid Metabolism and Gut Microbiota in Patients With Obesity

Probiotics Effect on Glucose and Lipid Metabolism and Gut Microbiota in Patients With Obesity: a Randomized, Double-blind Controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02733484
Enrollment
100
Registered
2016-04-11
Start date
2015-10-31
Completion date
2017-12-31
Last updated
2017-03-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity

Keywords

Obesity,Probiotics,Treatment

Brief summary

The purpose of this study is to determine whether the probiotics will be effective in the treatment of obesity

Detailed description

This study aims to evaluate the effect of probiotics on the improvement of glucose and lipid metabolism, as well as the gut microbiota.Baseline, 1 month and 3 months data will be collected and put into analysis to provide some suggestions on the probiotics use in the clinical practice for obesity patients.

Interventions

DIETARY_SUPPLEMENTProbiotics

the patients in this arm will receive probiotics with a dose for 2g/d for 3 months.

DIETARY_SUPPLEMENTPlacebo

the patients in this arm will receive placebo intervention

Sponsors

Shanghai 10th People's Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
15 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

1. Age 15-60 years 2. BMI≥28.0kg/m2 3. Agree to cooperate in the trial 4. Provision of written informed consent

Exclusion criteria

1. With chronic gastrointestinal diseases, severe immune deficiency, lactose intolerance 2. Diabetes 3. Use antibiotics, bacteriostatic agents (eg berberine), lipid-lowering drugs, antacids, H2 Blockers, proton pump inhibitors, corticosteroids or sex hormones 4. Use any probiotics in the last 3 months 5. Allergic constitution 6. Participating in any other clinical trials 7. Was not able to insist until the end 8. Pregnant and lactating women

Design outcomes

Primary

MeasureTime frameDescription
change from baseline in fasting blood-glucose at 1 month1 monthchange of the fasting blood-glucose will be calculated at 1 month in comparison with the baseline
change from baseline in fasting blood-glucose at 3 months3 monthschange of the fasting blood-glucose will be calculated at 3 months in comparison with the baseline
change from baseline in glycosylated hemoglobin change at 1 month1 monthchange of the glycosylated hemoglobin will be calculated at 1 month in comparison with the baseline
change from baseline in glycosylated hemoglobin change at 3 months3 monthschange of the glycosylated hemoglobin will be calculated at 3 months in comparison with the baseline

Secondary

MeasureTime frameDescription
change from baseline in percentage of body fat at 3 months3 months
change from baseline in gut microbiota at 1 month1 monthstudy the microbiota change of stool samples at 1 month in comparison with the baseline
change from baseline in gut microbiota at 3 months3 monthsstudy the microbiota change of stool samples at 3 months in comparison with the baseline
change from baseline in triglyceride at 1 month1 month
change from baseline in triglyceride at 3 months3 months
change from baseline in cholesterol at 1 month1 month
change from baseline in cholesterol at 3 months3 months
change from baseline in high-density lipoprotein at 1 month1 month
change from baseline in high-density lipoprotein at 3 months3 months
change from baseline in low-density lipoprotein at 1 month1 month
change from baseline in low-density lipoprotein at 3 months3 months
change from baseline in glutamic oxalacetic transaminase at 1 month1 month
change from baseline in glutamic oxalacetic transaminase at 3 months3 months
change from baseline in alkaline transaminase at 1 month1 month
change from baseline in alkaline transaminase at 3 months3 months
change from baseline in alkaline phosphatase at 1 month1 month
change from baseline in alkaline phosphatase at 3 months3 months
change from baseline in superoxide dismutase at 1 month1 month
change from baseline in superoxide dismutase at 3 months3 months
change from baseline in C-reactive protein at 1 month1 month
change from baseline in C-reactive protein at 3 months3 months
change from baseline in uric acid at 1 month1 month
change from baseline in uric acid at 3 months3 months
change from baseline in tumor necrosis factor-a at 1 month1 month
change from baseline in tumor necrosis factor-a at 3 months3 months
change from baseline in interleukin-6 at 1 month1 month
change from baseline in interleukin-6 at 3 months3 months
change from baseline in interleukin-8 at 1 month1 month
change from baseline in interleukin-8 at 3 months3 months
change from baseline in fasting insulin at 1 month1 month
change from baseline in fasting insulin at 3 months3 months
change from baseline in c peptide at 1 month1 month
change from baseline in visceral fat fraction at 3 months3 months
change from baseline in visceral fat fraction at 1 month1 month
change from baseline in c peptide at 3 months3 months
change from baseline in body age at 1 month1 month
change from baseline in body age at 3 months3 months
change from baseline in percentage of body fat at 1 month1 month

Countries

China

Contacts

Primary ContactCuiling Zhu, MD
1263856671@qq.com18817951953
Backup ContactRenyuan Gao, MD
renyuangao@126.com15601675695

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026