Skip to content

Research on probiotics in alleviating obesity and its accompanying intestinal dysfunction

Research on probiotics in alleviating obesity and its accompanying intestinal dysfunction

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200064291
Enrollment
Unknown
Registered
2022-10-02
Start date
2022-10-07
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

obesity

Interventions

Sunflower intervention group :Sunflower products
CCFM1062 Group:Bifidobacterium adolescentis CCFM1062
Competitive product group :Bifidobacterium animalis B420
placebo :placebo

Sponsors

Jiangnan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: ? 18 years old = age = 65 years old, male or female; ? BMI=26.0kg/m2 (refer to the Guidelines for the Prevention and Control of Overweight and Obesity in Chinese Adults); ? Stable body weight (±5 kg) within 6 months; ? Good diet, no high-fat and high-salt diet, no overeating or retaliatory eating, and no large-scale dieting; ? Make sure not to consume other weight loss drugs during this experiment; be willing not to consume other probiotics or fermented dairy products during this study, but still stick to previous eating habits; ? Good compliance, able to abide by the requirements of clinical trials; ? The subject or guardian has signed the informed consent; ? The patients fill in the written informed consent form, the International Physical Activity Scale and the Dietary Structure Questionnaire, and promise to cooperate with the research throughout the trial period.

Exclusion criteria

Exclusion criteria: ? Regular intake of antibiotics and corticosteroids, and vitamins within the past 6 months; ? Abuse of narcotics, psychotropic substances and cigarettes in the past 6 months; ? Rapid weight loss or gain in the past 6 months, malnutrition in daily food intake, total parenteral nutrition and protein malnutrition; ? During the study period or within the past 3 months, supplement nutrients such as probiotics and various minerals at least twice a week; ? Pregnant or lactating women, or planning to become pregnant in the next 6 months; ? No plan to lose weight or gain weight in the next 6 months; ? Allergy or intolerance to the ingredients of the test probiotic product; ? Poor patient compliance and poor possibility of follow-up;

Design outcomes

Primary

MeasureTime frame
BMI;

Secondary

MeasureTime frame
body fat percentage;Waist circumference;subcutaneous fat thickness;blood;Levels of liver; Analysis of gut microbiota;Analysis of metabolites;diet structure survey; International Physical Activity Scale;

Countries

China

Contacts

Public ContactFeng Zhang
wanggang@jiangnan.edu.cn15852818722

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026