dyslipidemi
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Patients with type 2 diabetes and hypertriglyceridemia who are treated in Hokkaido University or cooperated hospitals from June 2019 to March 2020. 2)Patients who are going to be treated with pemafibrate or switched from other fibrates to pemaribrate. 3)Patients who have been treated with fibrate without switching to pemafibrate or taking no medication over a year. 4) over 20 years old 5) Written informed consent
Exclusion criteria
Exclusion criteria: Patients who thought to be inappropriate to enter this study for some reasons by physician's judgments
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Changes of TG and HDL-C before and after administration of pemafibrate | — |
Secondary
| Measure | Time frame |
|---|---|
| 1)total lipid metabolism (remnant, sd-LDL, etc) 2)Liver function 3)Renal function 4)Body weight, Body mass index, Abdominal circumference 5)Fasting plasma glucose, HbA1c, insulin sensitivity and insulin secretion 6)Blood pressure 7)Adverse event 8)Influencing factors on lipid metabolism, liver/renal function, and glucose metabolism 9)Variation of blood and urinary examination including lipid metabolism, as well as abdominal ultrasound findings between pemafibrate group and control | — |
Countries
Japan
Contacts
Hokkaido University Faculty of Medicine and Graduate School of Medicine Division of Diabetes and Obesity