Dyslipidemia
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1)Those who have given their free and voluntary written consent to participate in this study. 2)Men and women who are 18 years of age or older at the time consent is obtained. 3)Persons who have lipid abnormalities or have been diagnosed with dyslipidemia 4)Patients whose fasting blood collection measurements in Visit 1 (SCR) meet any of the following. -LDL cholesterol 70 mg/dL or higher -HDL cholesterol less than 40mg/dL -TG 150 mg/dL or more, but less than 400 mg/dL 5)Patients who agree not to change the dosage and administration of the treatment for lipid disorders during the study period (V1 to V3).
Exclusion criteria
Exclusion criteria: 1)Patients with malignant tumors within the past 10 years 2)Persons deemed ineligible by the study physician
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To understand the actual status of the percentage of patients achieving the target values for the management of LDL-Cholesterol | — |
Secondary
| Measure | Time frame |
|---|---|
| The impact of communicating their own target values for the management of LDL-Cholesterol to dyslipidemic patients on various lipid parameters(LDL-C,HDLC,Non-HDL-C,TG). | — |
Countries
Japan
Contacts
TOKYO CENTER CLINIC Clinical Research Group