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Pitavastatin Evaluation of Atherosclerosis Regression by Intensive Cholesterol-Lowering Therapy (PEACE)

Not Applicable
Conditions
hyperlipidemia carotid artery atherosclerosis
Registration Number
JPRN-UMIN000001229
Lead Sponsor
Department of Cardiovascular Medicine, Kyoto Prefectural University of Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
300
Inclusion Criteria

Not provided

Exclusion Criteria

Subjects who received or are planned to receive intervention on carotid arteries during the study period Subjects with overt liver dysfunction (ALT; 100 IU/L and over) Subjects with overt renal dysfunction (serum creatinine; 2.0 mg/dL and over) Subjects receiving Cyclosporin Subjects hyperreactive to Pitavastatin Subjects with pregnancy or lactation

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
absolute changes in carotid intima-media thickness from baseline to final visit (12 months)
Secondary Outcome Measures
NameTimeMethod
relative change in carotid intima-media thickness change in LDL-C, HDL-C, TG and RLP-C change in hs-CRP and IL-6 new onset or recurrence of ischemic heart disease, heart failure, stroke and atherosclerosis obliterans sudden death side effects
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