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| Sponsor: | Kumamoto University |
|---|---|
| Information provided by: | Kumamoto University |
| ClinicalTrials.gov Identifier: | NCT00110448 |
Purpose
The purpose of this study is to determine the effects of low-dose aspirin for the primary prevention of vascular events in patients with type 2 diabetes in Japan.
| Condition | Intervention | Phase |
|---|---|---|
|
Coronary Disease Arteriosclerosis Diabetes Mellitus, Type 2 |
Drug: Aspirin Drug: No aspirin |
Phase IV |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Investigator, Outcomes Assessor) Primary Purpose: Prevention |
| Official Title: | Japanese Primary Prevention of Atherosclerosis With Aspirin for Diabetes (JPAD) Trial |
| Enrollment: | 2539 |
| Study Start Date: | December 2002 |
| Study Completion Date: | July 2008 |
| Primary Completion Date: | May 2008 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Active Comparator: 1
Aspirin use
|
Drug: Aspirin
Aspirin 81 mg or 100 mg per day
|
|
Active Comparator: 2
No aspirin use
|
Drug: No aspirin
No aspirin use
|
There is a worldwide epidemic of diabetes and the number of individuals with diabetes is set to increase further. As individuals with diabetes are at high risk of accelerated atherosclerosis and thrombotic vascular events, the significant proportion of the cardiovascular disease burden is projected to be among this population. JPAD is a multicenter study with a prospective randomized open, blinded end-point (PROBE) design. The doses administered are aspirin 81 mg/day or 100 mg/day, the latter being enteric-coated Aspirin.
The primary objective was to compare the effect of aspirin on atherosclerotic events including cardiovascular events, cerebral vascular event, and other vascular events.
We also analyze hemorrhagic events in this RCT.
Eligibility| Ages Eligible for Study: | 30 Years to 85 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| Japan | |
| First Department of Internal Medicine, Nara Medical University | |
| Kashihara, Nara, Japan, 634-8522 | |
| Department of Cardiovascular Medicine, Graduate School of Medical Sciences, Kumamoto University | |
| Kumamoto, Japan, 860-8556 | |
| Principal Investigator: | Hisao Ogawa, MD | Professor of Medicine, Department of Cardiovascular Medicine, Graduate School of Medical Sciences, Kumamoto University |
| Principal Investigator: | Yoshihiko Saito, MD | Professor of Medicine, First Department of Internal Medicine, Nara Medical University |
More Information
| Responsible Party: | Hisao Ogawa, Kumamoto University |
| ClinicalTrials.gov Identifier: | NCT00110448 History of Changes |
| Other Study ID Numbers: | H14-Kouka(Seikatsu)-025 |
| Study First Received: | May 9, 2005 |
| Last Updated: | September 22, 2008 |
| Health Authority: | Japan: Ministry of Health, Labor and Welfare |
|
type 2 diabetes coronary heart diseases primary prevention atherosclerosis aspirin |
|
Arteriosclerosis Atherosclerosis Coronary Disease Coronary Artery Disease Diabetes Mellitus Diabetes Mellitus, Type 2 Arterial Occlusive Diseases Vascular Diseases Cardiovascular Diseases Myocardial Ischemia Heart Diseases Glucose Metabolism Disorders Metabolic Diseases Endocrine System Diseases Aspirin |
Anti-Inflammatory Agents, Non-Steroidal Analgesics, Non-Narcotic Analgesics Sensory System Agents Peripheral Nervous System Agents Physiological Effects of Drugs Pharmacologic Actions Anti-Inflammatory Agents Therapeutic Uses Antirheumatic Agents Fibrinolytic Agents Fibrin Modulating Agents Molecular Mechanisms of Pharmacological Action Cardiovascular Agents Hematologic Agents |