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Effects of GLP-1 Receptor Agonists on Bile Acid Metabolism and Intestinal Microorganisms: Identification of Association with Nonalcoholic Fatty Liver

Effects of GLP-1 Receptor Agonists on Bile Acid Metabolism and Intestinal Microorganisms: Identification of Association with Nonalcoholic Fatty Liver

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0004923
Enrollment
22
Registered
2020-04-16
Start date
2019-09-18
Completion date
Unknown
Last updated
2020-04-21

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

Conditions

None listed

Interventions

Drug : For type 2 diabetes patients with insufficient blood glucose control with metformin and sulfonlyurea 2 therapy, the drug is 1:1 randomly assigned to the group Dulaglutide (GLP-1 receptor agonis

Sponsors

Kyung Hee University Hosipital at Gangdong
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 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

Exclusion criteria

Exclusion criteria: 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

Design outcomes

Primary

MeasureTime frame
Change in severity of fatty liver

Secondary

MeasureTime frame
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

Countries

Korea, Republic of

Contacts

Public Contactjunghwa Lee

Kyung Hee University Hosipital at Gangdong

Outcome results

None listed

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