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Evaluation of combination therapy with Statin and Ezetimible for patients with type II diabetes.

Evaluation of combination therapy with Statin and Ezetimible for patients with type II diabetes. - Evaluation of combination therapy with Statin and Ezetimible

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000002261
Enrollment
30
Registered
2009-07-28
Start date
2009-06-01
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

Pateients with type II diabetes combined with dyslipidemia

Interventions

Ezetimibe and Statin

Sponsors

Department of Cardiovascular Medicine, Saga University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: For entry into the study, participants must meet all of the following criteria. 1) Type II diabetes 2) Dyslipidemia given statin drug over 3 months. 3) At the time of entry, ezetimibe is not taken. 4) Age: 20years or older 5) Gender: regardless 6) Outpatient/hospitalized: regardless 7) Agreements: capable of giving consent and written agreement.

Exclusion criteria

Exclusion criteria: 1) Pregnant and/or breathfeeding, child-bearing potential women during this study. 2) Past history of severe allergic reactions to ezetimibe 3) Renal dysfunctioned. (ALT>2 x Normal range of each institute) 4) Uncontrolled diabetes mellitus (HbA1c>=9%) 5) Renal insufficiency (serum creatinine>2.0mg/dL) 6) Heart failure, cardiac infarct, unstable angina, or stroke whithin 3 months. 7) Recieving insulin therapy 8) Secondary hyperlipidemia and/or drug-induced hyperlipidemia 9) Familial hyperlipidemia 10) otherwise, treating physician judged not to be appropriate for inclusion in this study.

Design outcomes

Primary

MeasureTime frame
Examination of the rate change of glucouse metabolism and inflammatory marker Examination of ameliorating effect in kidney function

Secondary

MeasureTime frame
Examination of the rate change of TC, HDL cholesterol, and TG Decreasing rate of LDL cholesterol

Countries

Japan

Contacts

Public ContactKoichi Node, MD, PhD

Saga University Department of Cardiovascular Medicine

node@cc.saga-u.ac.jp0952-34-2364

Outcome results

None listed

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