Hypercholesterolemia
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients with hypercholesterolemia who have not attained the target LDL-C level established by the Japan Atherosclerosis Society guidelines for prevention of atherosclerotic cardiovascular diseases (2007). 2. Patients giving written consent on their own volition for participation in this clinical trial after being provided with sufficient explanation about the study.
Exclusion criteria
Exclusion criteria: 1. Patients who have a contraindication to LIVALO TAB administration. 2. Patients who have a contraindication to Zetia administration . 3. Patients who have a contraindication to LIPIDIL CAPSULE or Tricor Capsule administration. 4. Patients with liver dysfunction (AST or ALT values of >=100IU). 5. Patients being treated with statins. 6. Patients who are judged by the investigator to be not eligible for enrollment in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in atrial late potentials recorded by P wave signal-averaged ECG. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Correlation between baseline characteristics and atrial late potentials. 2. Correlation between change in atrial late potentials and change in blood biomarkers. | — |
Countries
Japan
Contacts
Osaka University Graduate School of Medicine Department of Advanced Cardiovascular Therapeutics