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Evaluation of eicosapentaenoic acid (EPA) for preventing the progression of coronary atherosclerosis and revascularization in patients with dyslipidemia who underwent percutaneous coronary intervention (PCI)

Evaluation of eicosapentaenoic acid (EPA) for preventing the progression of coronary atherosclerosis and revascularization in patients with dyslipidemia who underwent percutaneous coronary intervention (PCI) - Evaluation of EPA for preventing the progression of coronary sclerosis and revascularization in post-PCI patients with dyslipidemia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000003947
Enrollment
200
Registered
2010-07-26
Start date
2010-08-01
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

Coronary artery disease with dyslipidemia

Interventions

strong statin alone strong statin plus EPA 1800mg daily

Sponsors

Kurashiki central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Post-PCI patients with chronic coronary artery disease or acute coronary syndrome patients having >= 75% coronary artery stenosis according to the ACC/AHA classification 2) Patients with hypercholesterolemia taking strong statin or those meeting one of the dyslipidemia criteria: LDL-C >= 100mg/dl. TG >= 150mg/dl, HDL-C < 40mg/dl 3) Age: 20<=, < 75 years 4) Patients who can be followed up for longer than 18 months after PCI 5) Patients who have given written informed consent

Exclusion criteria

Exclusion criteria: 1) Patients who have hypersensitivity to EPA 2) Patients who had cerebral accident in the past 6 months 3) Pregnant women and women suspected of being pregnant 4) Patients with gastrointestinal ulcer in active phase 5) Patients with bleeding 6) Patients who have very poor choleresis or severe liver dysfunction 7) Patients who are ineligible for this study 8) Patients with severe renal dysfunction or undergoing dialysis

Design outcomes

Primary

MeasureTime frame
In non-PCI lesions with >= 50% stenosis according to the AHA classification, 1) change in MLD during the follow-up period 2) coronary revascularization

Secondary

MeasureTime frame
MACCE: death, nonfatal myocardial infarction, cerebral accident, unstable angina requiring hospitalization

Countries

Japan

Contacts

Public ContactYasushi Fuku

Kurashiki central Hospital Department of Cardiology

+81-86-422-0210

Outcome results

None listed

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