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临床试验/NCT00575172
NCT00575172已完成不适用

To Investigate Whether the Postprandial Blood Sugar Level as Achieved Using Ultrarapid-Acting Type Insulin Could Prevent Great Vessel Disorder in Japanese Type 2 Diabetic Patients.

Osaka Saiseikai Nakatsu Hospital1 个研究点 分布在 1 个国家目标入组 346 人开始时间: 2003年3月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
346
试验地点
1
主要终点
Cardiovascular events 1)Sudden death 2)New development or recurrence of apoplexy or TIA 3)New development or recurrence of AMI or and angina pectoris 4)Newly developed ASO, amputation of leg due to ASO

研究概览

简要总结

For the purpose of comparing efficacy of intensive therapy between 1) ultrarapid-acting type insulin (insulin aspart) and 2) conventional rapid-acting type insulin (R), a Multicenter Open Label Randomized Controlled Trial was planned in Japan using the occurrence of cardiovascular events in patients with diabetes, a high risk factor, as an index.

详细描述

A survey shows that the most frequently observed direct cause of death in diabetic patients is cardiovascular disorder. However, investigations and surveys such as DCCT, UKPDS and KUMAMOTO-study, etc. clarified that strict control of blood sugar level prevented development and progress of diabetic microangiopathy, but could not show a significant effect on great vessel disorder. Recently, the DECODA-study, DECODE-study and Honolulu-study have demonstrated that postprandial high blood sugar is involved in great vessel disorder. Therefore, possible prevention of great vessel disorder in diabetic patients is suggested by improving the postprandial blood sugar level as achieved using ultrarapid-acting type insulin, which has become available recently. Even with results in Europe and the US obtained, the life-style and incidence of complications in Japanese people are different, and there are many points that remain uncertain with respect to the direct application of foreign results to Japanese people. Therefore, in Japan also, it is necessary to conduct a large-scale clinical study and to establish high-level evidence using mainly Japanese people through hospitals having many patients.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
20 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Subjects are patients satisfying the following conditions 1) - 3).
  • Outpatients and inpatients aged 20 years or more but younger than 85 years. Men or women.
  • Patients with type 2 diabetes based on the diagnostic standard of the Japanese Diabetes Society
  • No specific restriction on the current treatment. Patients having switched treatment are also accepted.

排除标准

  • Patients with type 1 diabetes
  • Patients with a past history of cerebral angiopathy (cerebral hemorrhage, cerebral infarction, transient cerebral ischemic attack, subarachnoid hemorrhage, etc.) within 6 months before giving consent
  • Patients with a past history of myocardial infarction within 6 months before giving consent
  • Patients planning to receive PTCA or CABG, or who had PTCA or CABG within 6 months before giving consent
  • Patients with coronary arteriopathy (angina pectoris, etc.) that requires treatment with β-blocker or calcium-antagonist
  • Patients with atrial fibrillation or atrial flutter
  • Patients with renal dysfunction (serum creatinine ≥ 3.0 mg/dL)
  • Patients with liver dysfunction (AST, ALT ≥ 100 IU/L)
  • Patients with a past history or suspected of having a malignant tumor within 5 years before giving consent
  • Pregnant or possibly pregnant patients
  • Other patients judged inappropriate for the study by the investigators (patients presenting difficulty in frequently receiving rapid-acting type insulin or ultrarapid-acting type insulin therapy, including patients' compliance with treatment)

结局指标

主要结局

Cardiovascular events 1)Sudden death 2)New development or recurrence of apoplexy or TIA 3)New development or recurrence of AMI or and angina pectoris 4)Newly developed ASO, amputation of leg due to ASO

时间窗: five years

次要结局

  • 1)Total mortality 2)Changes in the mean IMT of common carotid arteries 3)Changes in the pulse wave velocity (PWV) (rt & 1t baPWV), ABI(five years)

研究者

申办方类型
Other

研究点 (1)

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