None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Age 18-45 years 2.18.5 = BMI =25 kg/m^2 3.All gender 4.Volunteers (including partners) have no planned pregnancy and are voluntarily taken from 14 days before screening to 6 months after the end of the trial .Take effective non-drug contraception. 5.Participants are willing to provide blood and fecal samples and fill out questionnaires through the entire study period.
Exclusion criteria
Exclusion criteria: 1.Intake of medicine 2.With lactose allergy or intolerance; 3.Intake of alcohol 4.Intake of antibiotic in previous 6 months 5.Daily consumption of >10 cigarettes, or >6 cups of coffee 6.Type 2 diabetes, hypertension, and fatty liver disease 7.Autoimmune disease 8.Internal disease including the gastrointestinal tract, lung, heart, vasculature, liver and kidney 9.Eating disorder or unconventional eating habits 10.Women: pregnancy and breastfeeding 11.In the opinion of the investigator, it cannot be enrolled
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Metagenomic Sequencing;16s rRNA Sequencing; | — |
Secondary
| Measure | Time frame |
|---|---|
| Blood Biochemical Values; | — |
Countries
China
Contacts
The 940th Hospital of Joint Logistics Support Force