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Study of high-dose Pitavastatin on lipid and glucose metabolism disorder in Coronary Artery Disease. (Shield-CAD)

Not Applicable
Recruiting
Conditions
Patients with stable coronary artery disease
Registration Number
JPRN-UMIN000008627
Lead Sponsor
Minami-Osaka Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
100
Inclusion Criteria

Not provided

Exclusion Criteria

Exclusion Criteria 1. Patients planed revascularization 2. Patients with occurrence of acute coronary syndrome (AMI or Unstable angina) within 3 months 3. Patients who have been undergone PCI or CABG within 3 months 4. Malignant tumor in active phase 5. Patients who have hypersensitivity to LIVALO, Lipitor, CRESTOR tablet 6) Patients who have severe liver dysfunction or biliary atresia. 7)Patients who are being treated with cyclosporine 8) Pregnant women, women suspected of being pregnant, or lactating women 9. Patients with prohibited drugs 10. Patients who received insulin therapy. 11. Patients who changed diabetes therapy within 3 months before entry. 12. Patients who received cholesterol-lowering agents except statin within a month before entry. 13. Patients undergoing dialysis 14. Patients with familial hypercholesterolemia 15. Patients who are ineligible in the opinion of the investigator

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Change and percent change in HbA1c at 3, 6 months after administration
Secondary Outcome Measures
NameTimeMethod
Change and percent change in TC, LDL-C, HDL-C, TG, Scr, microalbuminuria, eGFR, FBS, IRI, HOMA-IR, ApoA1, ApoB, ApoE and SAA at 3, 6, 9, 15 months after administration.
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