- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02733484
Probiotics Effect on Glucose and Lipid Metabolism and Gut Microbiota in Patients With Obesity
March 9, 2017 updated by: Huanlong Qin, Shanghai 10th People's Hospital
Probiotics Effect on Glucose and Lipid Metabolism and Gut Microbiota in Patients With Obesity: a Randomized, Double-blind Controlled Trial
The purpose of this study is to determine whether the probiotics will be effective in the treatment of obesity
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
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.
Study Type
Interventional
Enrollment (Anticipated)
100
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Cuiling Zhu, MD
- Phone Number: 18817951953
- Email: 1263856671@qq.com
Study Locations
-
-
Shanghai
-
Shanghai, Shanghai, China, 200072
- Recruiting
- Shanghai 10th People's Hospital
-
Contact:
- Cuiling Zhu, MD
- Phone Number: 18817951953
- Email: 1263856671@qq.com
-
Contact:
- Renyuan Gao, MD
- Email: renyuangao@126.com
-
Principal Investigator:
- Shen Qu, PhD
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
15 years to 60 years (Child, Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Age 15-60 years
- BMI≥28.0kg/m2
- Agree to cooperate in the trial
- Provision of written informed consent
Exclusion Criteria:
- With chronic gastrointestinal diseases, severe immune deficiency, lactose intolerance
- Diabetes
- Use antibiotics, bacteriostatic agents (eg berberine), lipid-lowering drugs, antacids, H2 Blockers, proton pump inhibitors, corticosteroids or sex hormones
- Use any probiotics in the last 3 months
- Allergic constitution
- Participating in any other clinical trials
- Was not able to insist until the end
- Pregnant and lactating women
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Probiotics
the patients in this arm will receive probiotics with a dose for 2g/d for 3 months.
|
the patients in this arm will receive probiotics with a dose for 2g/d for 3 months.
|
Placebo Comparator: Placebo
the patients in this arm will receive placebo with similar appearance of probiotics.
|
the patients in this arm will receive placebo intervention
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
change from baseline in fasting blood-glucose at 1 month
Time Frame: 1 month
|
change of the fasting blood-glucose will be calculated at 1 month in comparison with the baseline
|
1 month
|
change from baseline in fasting blood-glucose at 3 months
Time Frame: 3 months
|
change of the fasting blood-glucose will be calculated at 3 months in comparison with the baseline
|
3 months
|
change from baseline in glycosylated hemoglobin change at 1 month
Time Frame: 1 month
|
change of the glycosylated hemoglobin will be calculated at 1 month in comparison with the baseline
|
1 month
|
change from baseline in glycosylated hemoglobin change at 3 months
Time Frame: 3 months
|
change of the glycosylated hemoglobin will be calculated at 3 months in comparison with the baseline
|
3 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
change from baseline in gut microbiota at 1 month
Time Frame: 1 month
|
study the microbiota change of stool samples at 1 month in comparison with the baseline
|
1 month
|
change from baseline in gut microbiota at 3 months
Time Frame: 3 months
|
study the microbiota change of stool samples at 3 months in comparison with the baseline
|
3 months
|
change from baseline in triglyceride at 1 month
Time Frame: 1 month
|
1 month
|
|
change from baseline in triglyceride at 3 months
Time Frame: 3 months
|
3 months
|
|
change from baseline in cholesterol at 1 month
Time Frame: 1 month
|
1 month
|
|
change from baseline in cholesterol at 3 months
Time Frame: 3 months
|
3 months
|
|
change from baseline in high-density lipoprotein at 1 month
Time Frame: 1 month
|
1 month
|
|
change from baseline in high-density lipoprotein at 3 months
Time Frame: 3 months
|
3 months
|
|
change from baseline in low-density lipoprotein at 1 month
Time Frame: 1 month
|
1 month
|
|
change from baseline in low-density lipoprotein at 3 months
Time Frame: 3 months
|
3 months
|
|
change from baseline in glutamic oxalacetic transaminase at 1 month
Time Frame: 1 month
|
1 month
|
|
change from baseline in glutamic oxalacetic transaminase at 3 months
Time Frame: 3 months
|
3 months
|
|
change from baseline in alkaline transaminase at 1 month
Time Frame: 1 month
|
1 month
|
|
change from baseline in alkaline transaminase at 3 months
Time Frame: 3 months
|
3 months
|
|
change from baseline in alkaline phosphatase at 1 month
Time Frame: 1 month
|
1 month
|
|
change from baseline in alkaline phosphatase at 3 months
Time Frame: 3 months
|
3 months
|
|
change from baseline in superoxide dismutase at 1 month
Time Frame: 1 month
|
1 month
|
|
change from baseline in superoxide dismutase at 3 months
Time Frame: 3 months
|
3 months
|
|
change from baseline in C-reactive protein at 1 month
Time Frame: 1 month
|
1 month
|
|
change from baseline in C-reactive protein at 3 months
Time Frame: 3 months
|
3 months
|
|
change from baseline in uric acid at 1 month
Time Frame: 1 month
|
1 month
|
|
change from baseline in uric acid at 3 months
Time Frame: 3 months
|
3 months
|
|
change from baseline in tumor necrosis factor-a at 1 month
Time Frame: 1 month
|
1 month
|
|
change from baseline in tumor necrosis factor-a at 3 months
Time Frame: 3 months
|
3 months
|
|
change from baseline in interleukin-6 at 1 month
Time Frame: 1 month
|
1 month
|
|
change from baseline in interleukin-6 at 3 months
Time Frame: 3 months
|
3 months
|
|
change from baseline in interleukin-8 at 1 month
Time Frame: 1 month
|
1 month
|
|
change from baseline in interleukin-8 at 3 months
Time Frame: 3 months
|
3 months
|
|
change from baseline in fasting insulin at 1 month
Time Frame: 1 month
|
1 month
|
|
change from baseline in fasting insulin at 3 months
Time Frame: 3 months
|
3 months
|
|
change from baseline in c peptide at 1 month
Time Frame: 1 month
|
1 month
|
|
change from baseline in c peptide at 3 months
Time Frame: 3 months
|
3 months
|
|
change from baseline in visceral fat fraction at 1 month
Time Frame: 1 month
|
1 month
|
|
change from baseline in visceral fat fraction at 3 months
Time Frame: 3 months
|
3 months
|
|
change from baseline in body age at 1 month
Time Frame: 1 month
|
1 month
|
|
change from baseline in body age at 3 months
Time Frame: 3 months
|
3 months
|
|
change from baseline in percentage of body fat at 1 month
Time Frame: 1 month
|
1 month
|
|
change from baseline in percentage of body fat at 3 months
Time Frame: 3 months
|
3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Huanlong Qin, Shanghai 10th People's Hospital
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
October 1, 2015
Primary Completion (Anticipated)
December 1, 2017
Study Completion (Anticipated)
December 1, 2017
Study Registration Dates
First Submitted
April 5, 2016
First Submitted That Met QC Criteria
April 5, 2016
First Posted (Estimate)
April 11, 2016
Study Record Updates
Last Update Posted (Actual)
March 10, 2017
Last Update Submitted That Met QC Criteria
March 9, 2017
Last Verified
March 1, 2017
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- PTD02
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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