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Pioglitazone Protects Diabetes Mellitus (DM) Patients Against Re-Infarction (PPAR Study)

Primary Purpose

Diabetes Mellitus, Myocardial Infarction

Status
Terminated
Phase
Phase 4
Locations
Japan
Study Type
Interventional
Intervention
pioglitazone
control
Sponsored by
National Cerebral and Cardiovascular Center, Japan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Diabetes Mellitus focused on measuring diabetes mellitus, myocardial infarction, pioglitazone

Eligibility Criteria

20 Years - 79 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Arm Type

Active Comparator

Active Comparator

Arm Label

Pioglitazone

Control

Arm Description

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.

Outcomes

Primary Outcome Measures

The time till the first cardiovascular composite endpoint
death from cardiovascular death, and the hospitalization due to nonfatal myocardial infarction, nonfatal unstable angina25, treatment with coronary revascularisation (percutaneous coronary intervention or coronary artery bypass graft) and cerebral infarction.

Secondary Outcome Measures

All cause mortality
death of any cause
Hospitalization due to nonfatal myocardial infarction
nonfatal myocardial infarction
Hospitalization due to nonfatal unstable angina
nonfatal unstable angina
Hospitalization due to treatment with coronary revascularisation (percutaneous coronary intervention or coronary artery bypass graft)
coronary revascularisation
Hospitalization due to cerebral infarction
cerebral infarction
The progression of DM
HbA1C levels>7.0%
worsening of renal function
serum creatine levels>2.5mg/dL or the increases of serum creatine levels by >2mg/dL

Full Information

First Posted
September 13, 2005
Last Updated
May 22, 2018
Sponsor
National Cerebral and Cardiovascular Center, Japan
Collaborators
Japan Heart Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT00212004
Brief Title
Pioglitazone Protects Diabetes Mellitus (DM) Patients Against Re-Infarction (PPAR Study)
Official Title
The Japan Working Group for the Assessment That the Pioglitazone Protects DM Patients Against Re-Infarction
Study Type
Interventional

2. Study Status

Record Verification Date
May 2018
Overall Recruitment Status
Terminated
Why Stopped
Limited budget to continue this study
Study Start Date
April 2005 (Actual)
Primary Completion Date
April 2017 (Actual)
Study Completion Date
April 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
National Cerebral and Cardiovascular Center, Japan
Collaborators
Japan Heart Foundation

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
To evaluate whether the pioglitazone could reduce the recurrence of myocardial infarction (MI) in patients with DM and old myocardial infarction
Detailed Description
Type 2 diabetes mellitus is a well-established risk factor for coronary heart disease and atherosclerotic change in coronary artery. So we designed a prospective randomized multi-center trial named the pioglitazone could reduce the recurrence of myocardial infarction in patients with DM and myocardial infarction(PPAR study) to evaluate whether pioglitazone could reduce the recurrence of myocardial infarction in patients with DM(HbA1c<6.5%) and myocardial infarction. More than 100 hospitals will participate in the PPAR study. Patients with DM who have history of prior myocardial infarction are randomly allocated to receive pioglitazone or (1)instructs weight reduction, appropriate diet, regular exercise and/or (2)prescribes sulfonylurea agents. The number of patients to be recruited is 720 and this study will continue at least 2 years until 7 year or the end of the study. The primary end-points are (1) cardiovascular mortality and (2) hospitalization for cardiovascular events. Effects in suppression of new diabetes development also will be evaluated. We should recognize DM as important therapeutic target to decrease recurrence of cardiovascular events. PPAR study, a large scale multi-center trial in Japan, will provide us new evidence how to treat DM patients with prior myocardial infarction.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Myocardial Infarction
Keywords
diabetes mellitus, myocardial infarction, pioglitazone

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
630 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Pioglitazone
Arm Type
Active Comparator
Arm Description
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.
Arm Title
Control
Arm Type
Active Comparator
Arm Description
Participants assigned to Control group were treated with diet and exercise therapy or sulfonylurea (SU) or other additional drugs than pioglitazone.
Intervention Type
Drug
Intervention Name(s)
pioglitazone
Intervention Type
Other
Intervention Name(s)
control
Primary Outcome Measure Information:
Title
The time till the first cardiovascular composite endpoint
Description
death from cardiovascular death, and the hospitalization due to nonfatal myocardial infarction, nonfatal unstable angina25, treatment with coronary revascularisation (percutaneous coronary intervention or coronary artery bypass graft) and cerebral infarction.
Time Frame
2 years
Secondary Outcome Measure Information:
Title
All cause mortality
Description
death of any cause
Time Frame
2 years
Title
Hospitalization due to nonfatal myocardial infarction
Description
nonfatal myocardial infarction
Time Frame
2 years
Title
Hospitalization due to nonfatal unstable angina
Description
nonfatal unstable angina
Time Frame
2 years
Title
Hospitalization due to treatment with coronary revascularisation (percutaneous coronary intervention or coronary artery bypass graft)
Description
coronary revascularisation
Time Frame
2 years
Title
Hospitalization due to cerebral infarction
Description
cerebral infarction
Time Frame
2 years
Title
The progression of DM
Description
HbA1C levels>7.0%
Time Frame
2 years
Title
worsening of renal function
Description
serum creatine levels>2.5mg/dL or the increases of serum creatine levels by >2mg/dL
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
79 Years
Accepts Healthy Volunteers
No
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Masafumi Kitakaze, MD, PhD
Organizational Affiliation
National Cerebral and Cardiovascular Center, Japan
Official's Role
Study Chair
Facility Information:
Facility Name
National Cardiovascular Center
City
Suita
State/Province
Osaka
ZIP/Postal Code
565-8565
Country
Japan

12. IPD Sharing Statement

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Pioglitazone Protects Diabetes Mellitus (DM) Patients Against Re-Infarction (PPAR Study)

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