Type 2 diabetes mellitus
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients aged 18 years or older who received a new GLP-1 receptor agonist (Liraglutide, exenatide, lixisenatide, dulaglutide, semaglutide) or GIP/GLP-1 receptor agonist (tilzepatide) during the observation period. Gender includes both men and women.
Exclusion criteria
Exclusion criteria: 1. Patients with advanced-stage malignancies at the time of introduction of GLP-1 receptor agonists or GIP/GLP-1 receptor agonists. 2. Patients with active infection at the time of introduction of GLP-1 or GIP/GLP-1 receptor agonists. 3. Patients with reduced ADL at the time of introduction of GLP-1 or GIP/GLP-1 receptor agonists. 4. Patients with inadequate data from 4 weeks before initiation of GLP-1 receptor agonists or GIP/GLP-1 receptor agonists to 24 weeks after initiation. 5. Patients in whom another antidiabetic drug was added within 3 months prior to the observation period. 6. Other subjects judged by the research director to be inappropriate as research subjects. 7. Those who have expressed their intention to refuse participation by opting out.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Changes in HbA1c and body weight before and after initiation of GLP-1 receptor agonists or GIP/GLP-1 receptor agonists | — |
Countries
Japan
Contacts
Faculty of Internal Medicine, University of Miyazaki Division of Hematology, Diabetes, and Endocrinology,Department of Internal Medicine