Pioglitazone Protects Diabetes Mellitus (DM) Patients Against Re-Infarction (PPAR Study)
Diabetes Mellitus, Myocardial Infarction
About this trial
This is an interventional prevention trial for Diabetes Mellitus focused on measuring diabetes mellitus, myocardial infarction, pioglitazone
Eligibility Criteria
Inclusion Criteria: diabetes mellitus (fasting plasma glucose levels of>126 mg/dL, or 2-hour 75g oral glucose tolerance test (OGTT) value of >200 mg/dL, and HbA1c levels of<6.5% (47.5 IFCC)) History of myocardial infarction Age between 20-79 years old Exclusion Criteria: acute MI occurring within the last 7 days New York Heart Association (NYHA) symptoms of no fewer II or with left ventricular ejection fraction of not more than 40% suspected type I DM scheduled coronary angioplasty or history of coronary artery bypass graft surgery serious liver or kidney damage history of allergy or drug hypersensitivity arteriosclerosis obliterans with Fontaine stage III or worse inability to understand and/or comply with study medications, procedures and/or follow-up or any conditions that may render the patient unable to complete the study in the opinion of the investigator.
Sites / Locations
- National Cardiovascular Center
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
Pioglitazone
Control
Participants in the pioglitazone group were administered a pioglitazone tablet (15 mg) once a day. In the event of the side effects such as oedema, the dosage of pioglitazone was reduced to half or a quarter of the original dosage. Otherwise, we tried to increase the dose of pioglitazone to 30mg/day.
Participants assigned to Control group were treated with diet and exercise therapy or sulfonylurea (SU) or other additional drugs than pioglitazone.