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Prospective analysis of ComparIson of pReventive effect on CardiovascuLar Events with different statin therapy (P-CIRCLE)

Prospective analysis of ComparIson of pReventive effect on CardiovascuLar Events with different statin therapy (P-CIRCLE) - Prospective analysis of ComparIson of pReventive effect on CardiovascuLar Events with different statin therapy (P-CIRCLE)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000008042
Enrollment
660
Registered
2012-05-28
Start date
2012-06-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients with coronary artery disease who underwent PCI

Interventions

Pitavastatin 2~4mg daily Atorvastatin 10~20mg daily

Sponsors

Kawasaki Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Patients with hypercholesterolemia who satisfied each criteria below -LDL-C level is equal or greater than 100 mg/dL -requiring cholesterol lowering drugs judged by attending physicians 2.Patients given written informed consent

Exclusion criteria

Exclusion criteria: 1.Patients who met contraindication of LIVALO tablet below - Patients who have hypersensitivity to LIVALO tablet -Patients who have severe liver dysfunction or biliary atresia. -Co-administration with cyclosporine -Women who are pregnant or may become pregnant or nursing mothers 2.Patients who meet contraindication of LIPITOL tablet below - Patients who have hypersensitivity to LIPITOL tablet -Patients with the following diseases considered to be associated with defective hepatic metabolism: acute hepatitis, acute exacerbation of chronic hepatitis, liver cirrhosis, hepatic carcinoma and/or icterus -Women who are pregnant or may become pregnant or nursing mothers 3.Patients with hepatic disorders (ALT or AST level is equal or greater than 100IU/L) 4.Patients who are ineligible in the opinion of the investigator

Design outcomes

Primary

MeasureTime frame
Composite cardiovascular events Occurrence of one of following events 1.Cardiovascular death 2.Non-fatal Myocardial Infarction (MI) 3.Non-fatal Cerebral Infarction (CI) 4.Repeated revascularization including bypass surgery, target lesion revascularization and repeated PCI for de novo lesion

Countries

Japan

Contacts

Public ContactTakao Maruyama

Kawasaki Hospital Department of Cardiology

maruyama_takao@kawaswaki-hospital-kobe.or.jp078-511-3131

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026