Effects of GLP-1 Receptor Agonists on Bile Acid Metabolism and Intestinal Microorganisms: Identification of Association with Nonalcoholic Fatty Liver
- Conditions
- Endocrine, nutritional and metabolic disease
- Registration Number
- KCT0004923
- Lead Sponsor
- Kyung Hee University Hosipital at Gangdong
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 22
1) Adults between 20 and 75 years of age diagnosed with type 2 diabetes
2) Patients with poor control of blood sugar level of 7.0% or more of HbA1c even though metformin and sulfone urea were used in combination for more than 2 months
3) Those who voluntarily agreed to participate in the study
a. If you have a liver disease of a specific cause, such as viral hepatitis, autoimmune hepatitis, alcoholic liver disease
b. Drug users who can affect blood sugar, fatty liver, and gut microflora
(Within 3 months from the study start date)
-Glycocorticoid
-Nonsteroidal anti-inflammatory
-Immunosuppressive
-All kinds of antibiotics
-DPP4 inhibitors
-alpha glucosidase inhibitors
-Probiotics
-Hepatotonics, including UDCA
c. If the laboratory test results below are abnormal
-estimated GFR <30 ml / min / 1.73 m2
d. Drug abuser
e. Pregnant and lactating women
f. People on dialysis for terminal renal failure
g. Beneficiaries of organ transplants, including the liver
h. Those who have undergone surgery to modify the structure of the intestine (eg gastrointestinal resection)
i. 30g men a day, 20g women or more drinkers
j. Those who have received clinical trial drugs within the last 3 months
k. In addition, those judged to be impossible to participate
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Change in severity of fatty liver
- Secondary Outcome Measures
Name Time Method Changes in body mass index, waist circumference and body mass;Comparison before and after treatment of fasting blood glucose, glycated albumin, glycated hemoglobin;internal fat area change;Changes in insulin resistance and secretion;Change of Lipid profile;Change of AST, ALT, Total bilirubin;Change of hs-crp, leptin, adiponectin, TNF-a, IL-6;Change of primary bile acid and secondary bile acid;Comparison of microbial cluster changes in intestinal excretion