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The effects of ezetimibe and atorvastatin in acute coronary syndrome (ZEUS study)

The effects of ezetimibe and atorvastatin in acute coronary syndrome (ZEUS study) - ZEUS Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000002722
Enrollment
70
Registered
2009-11-28
Start date
2009-01-01
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

Acute Coronary Syndrome

Interventions

Ezetimibe 10mg daily Atorvastatin 10mg daily

Sponsors

Department of Cardiovascular Medicine, Juntendo University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The ethical committee of all participation center approved the protocol and all patients provided written informed consent.This study will be included men and women>=20 years of age with clinical diagnosis of acute coronary syndrome (ACS) who will meet IVUS criteria

Exclusion criteria

Exclusion criteria: 1,Advanced liver dysfunction 2,Renal failure 3,LDL cholesterol Level<100mg/dl 4,Any other reason for exclusion

Design outcomes

Primary

MeasureTime frame
the percent change in coronary plaque volume

Secondary

MeasureTime frame
1) absolute change from baseline in coronary plaque volume, (2) absolute change from baseline in coronary plaque stabilization(3)absolute and percent change in serum lipid and apolipoproteins (4) percent change in cholesterol absorption and synthesis markers (5)Correlation oflipid parameters and percent change in coronary plaque volume/stabilization (6) percent change in inflammatory marker and white blood cell count, (7) absolute and percent change in the coronary plaque area at the site of PCI, (8) absolute and percent change in MLD and %stenosis at the site of PCI, (9) major adverse cardiovascular event (MACE: defined as cardiac death, Q or non-Q wave myocardial infarction or TVR), (10) death, (11) any adverse incidents including changes in laboratory values

Countries

Japan

Contacts

Public ContactKatsumi Miyauchi

Juntendo University School of Medicine Department of Cardiovascular Medicine

03-3813-3111

Outcome results

None listed

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