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Effects of probucol and EPA on lipid component of HDL particles

Not Applicable
Conditions
Familial Hypercholesterolemia Dyslipidemia
Registration Number
JPRN-UMIN000024187
Lead Sponsor
Cardiology, Osaka University Graduate School of Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
30
Inclusion Criteria

Not provided

Exclusion Criteria

(A)Probucol-treated group 1)Taken probucol previously 2)Taking cyclosporin 3)Allergic to probucol 4)TG>400 mg/dL 5)HbA1c>8% 6)Frequent multifocal premature ventricular contraction 7)Atrial fibrillation 8)QTc>450msec(male),>470msec(female)on the ECG 9)Congestive heart failure or unstable angina 10)Participating in other trials 11)Pregnant (or might be pregnant) or lactating 12)The doctor decided to be inadequate for participating in this trial (B) EPA-treated group 1)Hemodialysis 2)Liver dysfunction 3)Active malignant diseases 4)Scheduled to undergo coronary angiography or CABG 5)Severe heart failure 6)ACS within 3 months 7)PCI or CABG within 3 months 8)HbA1c>8% 9)Secondary dyslipidemia or taking omega3 agents 10)Bleeding or bleeding tendency 11)Having past side effects for omega3 agents 12)Participating in other trials 13)Pregnant (or might be pregnant) or lactating 14)The doctor decided to be inadequate for participating in this trial

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Changes of lipid species in HDL particles after the treatment of probucol or EPA
Secondary Outcome Measures
NameTimeMethod
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