None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Voluntarily agree to participate and sign in informed consent form 2) Adults over 20 ages 3) BMI: = 23kg/m2 4) Blood glucose level at 30 minutes after oral glucose loading = 140mg/dl 5) A subjective symptom of irritable bowel syndrome
Exclusion criteria
Exclusion criteria: 1) Continuous consumption of dietary supplement or oriental medicine within 4 weeks before the first visit 2) Inflammatory disease or current consumption of insulin, antiinflammatory analgesic drug, antibiotic, anticoagulant, ACE inhibitor, angiotensin ?antagonist 3) Participation in other human study within 30days before the first visit 4) Pregnant or lactating women 5) Alcoholic 6) Following diseases : Heart failure, Coronary artery disease, Uncontrolled hypertension, Liver dysfunction, Renal dysfunction, Malignant tumors , Mental disease 7) Hypersensitivity to probiotics 8) Any condition that the principal investigator believes may put the subjects at undue risk
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Oral glucose tolerance test | — |
Secondary
| Measure | Time frame |
|---|---|
| Lactobacillus gasseri BNR17 concentration in feces;Interleukin-10 level in feces ;Bowel movement habit and satiety questionnaire | — |
Countries
Korea, Republic of
Contacts
Ewha Womans University