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The effects of ezetimibe on malondialdehyde-modified low-density lipoprotein in abnormal glucose tolerance patients with coronary artery disease

The effects of ezetimibe on malondialdehyde-modified low-density lipoprotein in abnormal glucose tolerance patients with coronary artery disease - The effects of ezetimibe on MDA-LDL in abnormal glucose tolerance patients with coronary artery disease

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000005078
Enrollment
40
Registered
2011-02-15
Start date
2008-10-01
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

Coronaty artery disease with diabetes, including impaired glucose torelance

Interventions

Administration of atorvastatin 20mg in the first 3 months, followed by the administration of atorvastatin 10mg and ezetimibe 10mg Administration of atorvastatin 10mg and ezetimibe 10mg in the first 3

Sponsors

Cardiovascular Center, Anjo Kosei Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients who have a history of following coronary heart diseases; CABG or PCI was performed more than 6 months before >= 50% coronary artery stenosis according to the ACC/AHA classification was found by CAG 2) Diabetic patients under treatment or patients who diagnosed with diabetic (inclucing IGT; 2-hour plasma/serum glucose level: 140mg/dL to 199mg/dL) at 75g oral glucose tolerance test 3) Patients who take atorvastatin 10mg more than 3 months 4) Patients who are judged to require the more lipid-lowering therapy

Exclusion criteria

Exclusion criteria: 1) Patients with history of acute coronary syndrome within 6 months 2) Patients with inflammatory disease, infectious disease, and malignancy 3) Patients with history of hypersensitivity against ezetimibe and atorvastatin 4) Pregnant women, women who may be pregnant, and breast-feeding women. 5) Patients with severe liver dysfunction or renal dysfunction 6) Insulin-treated diabetic patients 7) Patients judged by the investigator/ sub investigator to be ineligible for some other reason

Design outcomes

Primary

MeasureTime frame
Change and percent change in MDA-LDL

Secondary

MeasureTime frame
Change and percent change in TC, LDL-C, TG, and HDL-C. Change and percent change in HbA1c

Countries

Japan

Outcome results

None listed

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